LOOSE KERNEL SMUT- sporisorium cruentum solution 
LOOSE SMUT, WHEAT- ustilago tritici solution 
BARLEY LOOSE SMUT- ustilago nuda solution 
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES- mucor circinelloides f. circinelloides solution 
PAECILOMYCES VARIOTII- paecilomyces variotii solution 
ASPERGILLUS FUMIGATUS- aspergillus fumigatus solution 
RHIZOPUS STOLONIFER- rhizopus stolonifer solution 
SACCHAROMYCES CEREVISIAE- saccharomyces cerevisiae solution 
TRICHOPHYTON MENTAGROPHYTES- trichophyton mentagrophytes solution 
TRICHOPHYTON RUBRUM- trichophyton rubrum solution 
TRICHOTHECIUM ROSEUM- trichothecium roseum solution 
ALTERNARIA ALTERNATA- alternaria alternata solution 
ASPERGILLUS FLAVUS- aspergillus flavus solution 
ASPERGILLUS NIGER- aspergillus niger solution 
CHAETOMIUM GLOBOSUM- chaetomium globosum solution 
MOLD MIX 3- alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution 
ASPERGILLUS MIX- aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution 
DEMATIACEAE MIX- alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution 
NEW STOCK FUNGI MIX- acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution 
NEW STOCK FUNGI MIX- acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution 
GRASS SMUT MIX- ustilago cynodontis and sporisorium cruentum solution 
DRECHSLERA SPICIFERA- drechslera spicifera solution 
FUSARIUM MIX- gibberella fujikuroi and fusarium solani solution 
MUCOR MIX- mucor circinelloides f. lusitanicus and mucor plumbeus solution 
MOLD MIX 2- aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution 
MOLD MIX 1- alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution 
RHIZOPUS MIX- rhizopus stolonifer and rhizopus oryzae solution 
GLIOCLADIUM VIRIDE- gliocladium viride solution 
MOLD MIX 2- aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution 
AHH MOLD MIX- alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution 
ALTERNARIA/HORMODENDRUM MIX- alternaria alternata and aspergillus fumigatus solution 
ALTERNARIA HORMODENDRUM MIX- alternaria alternata and aspergillus fumigatus solution 
HELMINTHOSPORIUM SOLANI- helminthosporium solani solution 
MUCOR PLUMBEUS- mucor plumbeus solution 
ASPERGILLUS NIDULANS- aspergillus nidulans solution 
AUREOBASIDIUM PULLULANS- aureobasidium pullulans solution 
BIPOLARIS SOROKINIANA- bipolaris sorokiniana solution 
PENICILLIUM MIX- penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution 
GRASS SMUT MIX- ustilago cynodontis and sporisorium cruentum solution 
GRAIN SMUT MIX- ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution 
CANDIDA ALBICANS- candida albicans solution 
CORN SMUT- ustilago maydis solution 
PENICILLIUM CHRYSOGENUM (NOTATUM)- penicillium chrysogenum (notatum) solution 
TRICHODERMA HARZIANUM- trichoderma harzianum solution 
ALTERNARIA/HORMODENDRUM MIX- alternaria alternata and aspergillus fumigatus solution 
ACREMONIUM STRICTUM- acremonium strictum solution 
MONILIA MIX- candida albicans and neurospora intermedia solution 
NEUROSPORA INTERMEDIA- neurospora intermedia solution 
PENICILLIUM DIGITATUM- penicillium digitatum solution 
ASPERGILLUS MIX- aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution 
EPICOCCUM NIGRUM- epicoccum nigrum solution 
RHIZOPUS ORYZAE- rhizopus oryzae solution 
STEMPHYLIUM SOLANI- stemphylium solani solution 
MUCOR CIRCINELLOIDES F. LUSITANICUS- mucor circinelloides f. lusitanicus solution 
EPIDERMOPHYTON FLOCCOSUM- epidermophyton floccosum solution 
MICROSPORUM CANIS- microsporum canis solution 
BERMUDA GRASS SMUT- ustilago cynodontis solution 
FUSARIUM MONILIFORME- fusarium moniliforme solution 
ASPERGILLUS AMSTELODAMI- aspergillus amstelodami solution 
FUSARIUM SOLANI- fusarium solani solution 
PHOMA BETAE- phoma betae solution 
BOTRYTIS CINEREA- botrytis cinerea solution 
CLADOSPORIUM HERBARUM- cladosporium herbarum solution 
MYCOGONE PERNICIOSA- mycogone perniciosa solution 
CLADOSPORIUM SPHAEROSPERMUM- cladosporium sphaerospermum solution 
GEOTRICHUM CANDIDUM- geotrichum candidum solution 
OAT SMUT- ustilago avenae solution 
MOLD MIX 1- alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution 
RHODOTORULA MUCILAGINOSA- rhodotorula mucilaginosa solution 
PENICILLIUM MIX- penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution 
PHYCOMYCETES MIX- mucor circinelloides f. lusitanicus and rhizopus stolonifer solution 
Greer Laboratories, Inc.

----------

Non Standardized Allergenic Extracts
Pollens, Molds, Epidermals, Insects, Dusts, Foods, and Miscellaneous Inhalants

WARNING

THIS ALLERGENIC PRODUCT IS INTENDED FOR USE BY PHYSICIANS WHO ARE EXPERIENCED IN THE ADMINISTRATION OF ALLERGENIC EXTRACTS AND THE EMERGENCY CARE OF ANAPHYLAXIS, OR FOR USE UNDER THE GUIDANCE OF AN ALLERGY SPECIALIST.

ALLERGENIC EXTRACTS MAY CAUSE SEVERE OR FATAL ANAPHYLAXIS IN EXTREMELY SENSITIVE PATIENTS. THE INITIAL DOSE MUST BE BASED ON SKIN TESTING AS DESCRIBED IN THE DOSAGE AND ADMINISTRATION SECTION OF THIS INSERT. PATIENTS SHOULD BE INSTRUCTED TO RECOGNIZE ADVERSE REACTION SYMPTOMS AND CAUTIONED TO CONTACT THE PHYSICIAN'S OFFICE IF REACTION SYMPTOMS OCCUR. IN CERTAIN INDIVIDUALS, THESE REACTIONS COULD BE FATAL. PATIENTS SHOULD BE OBSERVED FOR AT LEAST 20 MINUTES FOLLOWING TREATMENT.

EMERGENCY MEASURES, AS WELL AS PERSONNEL TRAINED IN THEIR USE, SHOULD BE IMMEDIATELY AVAILABLE IN THE EVENT OF A LIFE‑ THREATENING REACTION. PATIENTS BEING SWITCHED FROM ONE LOT OF EXTRACT TO ANOTHER FROM THE SAME MANUFACTURER SHOULD HAVE THEIR DOSE REDUCED BY 75%.

THIS PRODUCT SHOULD NOT BE INJECTED INTRAVENOUSLY.

REFER ALSO TO THE WARNINGS, PRECAUTIONS, ADVERSE REACTIONS AND OVERDOSAGE SECTION BELOW.

Allergenic Extracts are supplied as a sterile solution for intracutaneous or subcutaneous administration. Concentrates contain the soluble extractants of the source material with 0.5% sodium chloride and 0.54% sodium bicarbonate at a pH of 6.8 to 8.4 as aqueous extracts in water for injection or in 50% glycerin. Aqueous extracts contain 0.4% phenol as a preservative and 50% glycerinated extracts contain 0.2% phenol. Diluted aqueous extracts contain Buffered Saline with 0.5% sodium chloride, 0.04% potassium phosphate, 0.11% sodium phosphate heptahydrate, and 0.4% phenol in water for injection.

Source materials for these extracts are as follows: Pollens are collected from the respective grasses, weeds, trees, shrubs, cultured plants and flowers. Mold extracts are produced from pure culture mycelial mats. Rusts and smuts are obtained from natural growths. Epidermal extracts are produced from the hide, hair, or feathers containing the natural dander, or from separated dander. Insects are the whole body insects. House dust is made from various dusts ordinarily found in the home with the extract dialyzed to remove low‑molecular weight irritants and concentrated to an extraction ratio of 1:1. Food extracts are prepared from the edible portions of the respective foods, obtained fresh if possible. Certain diagnostic food extracts contain 0.1% sodium formaldehyde sulfoxylate as an antioxidant. Other miscellaneous inhalants involved in respiratory allergy are obtained in the naturally occurring form to which a patient may be exposed.

Extracts are labeled either by weight‑to‑volume (w/v) based on the weight of the source material to the volume of the extracting fluid, or in protein nitrogen units (PNU) based on assay with one PNU representing 0.00001 mg of protein nitrogen.

The allergic reaction is dependent upon the presence of antigen‑specific immunoglobulin E (IgE) antibodies that are bound to specific receptors on mast cells and basophils. The presence of IgE antibodies on mast cells and basophils sensitizes these cells and, upon interaction with the appropriate allergen, histamine and other mediators are released. IgE antibody has been shown to correlate with atopic diseases such as allergic rhinitis and allergic asthma. (1‑4) In the skin these mediators are responsible for the characteristic wheal and flare (erythema) reactions upon Allergenic Extract skin testing in persons with the specific allergies. (3‑7)

Specific immunotherapy with Allergenic Extracts as employed for over 45 years is helpful in reducing symptoms associated with exposure to the offending allergens. A summary of effectiveness by the Panel on Review of Allergenic Extracts, an advisory committee to the U.S. Food and Drug Administration, has been published. (8) Several mechanisms have been proposed to explain the effectiveness of immunotherapy: an increase in antigen‑specific IgG antibodies is frequently associated with clinical effectiveness, although correlation is not consistent in all studies; there is a decrease in specific IgE; and IgE production is suppressed during periods of seasonal or high exposure to the antigen. (9) Other changes following immunotherapy have been noted including development of auto‑anti‑idiotypic antibodies; a decrease in blood basophil sensitivity to allergen; a decrease in lymphokine production and lymphocyte proliferation by cells exposed to allergen; and development of allergen‑specific suppressor cells. (10) The complete mechanisms of immunotherapy are not known and remain the subject of investigation.

Allergenic Extracts are indicated for the diagnosis and treatment of patients with immediate hypersensitivity allergy to the respective allergens, inhaled, ingested or otherwise introduced into contact with sensitive tissues. The diagnosis of IgE‑mediated allergy may be established by the allergy history, clinical evaluation, and skin test reactivity. (4,7,11) Immunotherapy with Allergenic Extracts is indicated when testing and patient history have identified the offending allergens and when it is not possible or practical to avoid these allergens. (12‑14) Food extracts have not been proven effective in immunotherapy.

The use of Allergenic Extracts for the above purposes should be made only by physicians with special familiarity and knowledge of allergy. (See DOSAGE AND ADMINISTRATION)

There are no known absolute contraindications to the use of Allergenic Extracts for immunotherapy. Immunotherapy with specific antigens should not be done in those individuals who do not exhibit skin test or clinical sensitivity to the particular antigens. (See below under WARNINGS and PRECAUTIONS)

Allergenic extract injections should not be administered in the presence of diseases characterized by a bleeding diathesis.

Children with nephrotic syndrome require careful consideration and probably should not receive injection therapy because a variety of seemingly unrelated events, such as immunization, can cause an exacerbation of their nephrotic disease.

General contraindications include:

EXTREME SENSITIVITY TO THE SPECIFIC ALLERGEN ‑ Determined from previous anaphylaxis following exposure.

AUTOIMMUNE DISEASE ‑ Individuals with autoimmune disease may be at risk, due to the possibility of routine immunizations exacerbating symptoms of the underlying disease.

Concentrated extracts must be diluted with a sterile diluent prior to first use on a patient for treatment or intradermal testing. Allergenic Extracts are manufactured to assure high potency and have the ability during skin testing and immunotherapy to cause serious local and systemic reactions including death in sensitive patients. Most reactions occur within 20 minutes after injection, (15) but may occur later. (16) To minimize the potential for local or systemic reactions, the relative sensitivity of the patient must be assessed from the allergic history and from clinical observations. Patients should be informed of these risks prior to skin testing and immunotherapy (see PRECAUTIONS and ADVERSE REACTIONS below).

Allergenic Extract immunotherapy doses should be lowered or temporarily withheld from patients if any of the following conditions exist:

(1) severe symptoms of rhinitis and/or asthma

(2) infection or flu accompanied by fever

(3) exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection

(4) evidence of a local or systemic reaction to the preceding extract injection during a course of immunotherapy

The dosage must be reduced when modifying dosages or components in a mixture or an individual prescription, or when starting a patient on fresh extract, even though the labeled strength of the old and new vials may be the same. This reduction in dosage may be necessary due to the older vial losing potency during storage, or due to different sensitivities to different components. The amount of new extract given should not exceed 25% of the last dose given from the old vial, assuming both extracts contain comparable amounts of allergen. Any evidence of a local or generalized reaction requires a reduction in dosage during the initial stages of immunotherapy, as well as during maintenance therapy.

GENERAL:

Not for intravenous use!

Systemic allergic reactions may occur as a result of immunotherapy. The risk can be minimized by adherence to a careful injection schedule, which starts with a low concentration of extract and is increased slowly. Because of the danger of serious reactions, caution is needed in testing exquisitely sensitive patients, particularly with potent allergens, e.g., peanut, cottonseed, and flaxseed. (8) Such extracts should be appropriately diluted before use.

The physician must be prepared to treat anaphylaxis should it occur and have the necessary drugs and equipment on hand to do so. (17‑18) Extracts should not be administered by the patient or other individuals who are not prepared to treat anaphylaxis should it occur.

Patients receiving Allergenic Extracts should be kept under observation a minimum of twenty (20) minutes so that any adverse reaction can be observed and properly handled. (15) This time should be extended for high‑risk patients such as those with unstable asthma or those suffering an exacerbation of their symptoms.

Patients receiving beta blockers may not be responsive to beta adrenergic drugs used to treat anaphylaxis. The risks of anaphylaxis in these patients should be carefully weighed against the benefits of immunotherapy.

Check the lot number and dosage schedule of the patient to verify correctness of a prescription number, a vial number, or strength. Only after this verification has been made should an injection be given.

A separate sterile needle and syringe should be used for each patient to prevent transmission of hepatitis or other infectious agents.

INFORMATION FOR PATIENTS:

Most serious reactions following the administration of Allergenic Extracts occur within 20 minutes; the patient should remain under observation for this period of time or longer if instructed by the physician. The size of any local reaction should be recorded, because increasingly large local reactions may precede a subsequent systemic reaction with increasing dosage. The patient should be instructed to report any unusual reactions. In particular, this includes unusual swelling and/or tenderness at the injection site, or reactions such as rhinorrhea, sneezing, coughing, wheezing, shortness of breath, nausea, dizziness, or faintness. Reactions may occur some time after leaving the physician's office, in which case medical attention should be sought immediately.

DRUG INTERACTIONS: Skin test diagnosis with Allergenic Extracts is contraindicated within 24 hours after the last dose of most antihistamines, within 48 hours after the last dose of terfenadine, and within 3 weeks or longer after the last dose of astemizole. These products suppress histamine skin test reactions and could mask a positive response.

CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: There is no evidence of carcinogenicity, mutagenesis or impairment of fertility in humans from Allergenic Extracts. No long‑term studies in animals have been performed to evaluate carcinogenic potential.

PREGNANCY: PREGNANCY CATEGORY C ‑ Animal reproduction studies have not been conducted with Allergenic Extracts. It is also not known whether Allergenic Extracts can cause fetal harm when administered to a pregnant woman or whether they can affect reproduction capacity. Allergenic Extracts should be given to a pregnant woman only if clearly needed.

There is no evidence of adverse effects of Allergenic Extracts on the fetus. (8) Studies have not been performed in animals to determine whether extracts affect fertility in males or females, have teratogenic potential, or have other adverse effects on the fetus. Caution should be exercised in testing or treating pregnant females because a systemic reaction may cause an abortion as a result of uterine muscle contractions.

LABOR AND DELIVERY: There is no known information of adverse effects during labor and delivery.

NURSING MOTHERS: It is not known whether this product is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when extracts are administered to a nursing woman.

PEDIATRIC AND GERIATRIC USE: Although most extracts have not been studied systematically in children, children and geriatric patients appear to tolerate injections of Allergenic Extracts well. Studies with pollenosis and asthma have been conducted in children (e.g. refs. 19‑21). Extract usage in children should follow the same precautions as in adults.

Adverse systemic reactions may occur within minutes upon use of an Allergenic Extract to which a person has specific sensitivity. These reactions consist primarily of allergic symptoms such as generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, and hypotension. Less commonly, nausea, emesis, abdominal cramps, diarrhea and uterine contractions may occur. Severe reactions may cause shock and loss of consciousness. Fatalities have occurred rarely. (8,22,23) These systemic reactions occur with varying frequency in different clinics and are usually less than 1%. To some extent, the reaction rate is related to the type and dose of administered extract and to the sensitivity of the patient. In general, immunotherapy with Allergenic Extracts is considered to be safe. (24) Despite all precautions, occasional reactions are unavoidable.

Adverse systemic reactions should be treated as follows:

A. A tourniquet should be immediately applied to the extremity above the site of injection. Release the tourniquet every few minutes for a few seconds.

B. Epinephrine 1:1000 should be injected immediately in the opposite arm in amounts of 0.3 to 0.5 mL and 0.2 mL epinephrine should be administered at the site of injection. For children below the age of 6 years, adjust the dosage of epinephrine to 0.005 mL per pound of body weight per dose. Repeat epinephrine dosage in 15 minutes if necessary and if symptoms persist.

C. Adverse reactions not responding to epinephrine therapy may require the use of parenteral bronchodilators, vasopressors, oxygen, or volume replacement therapy.

Local reactions consisting of erythema, itching, swelling, tenderness and sometimes pain may occur at the injection site. These reactions may appear within a few minutes to hours and persist for several days. Local cold applications and oral antihistamines may be effective treatment. For marked and prolonged local reactions, steroids may be helpful.

Systemic reactions are uncommon after injection, but if the patient receives more extract than can be tolerated at that particular time and begins to experience immediate hypersensitivity anaphylaxis, the procedures listed under ADVERSE REACTIONS should be instituted.

Overdosage may occur because of an error in the volume of extract injected, or an incorrect dilution injected, or because the patient may be exposed to airborne or environmental antigens simultaneously with injection of the same antigens. In the event of a systemic reaction occurring, the dosage schedule should be carefully adjusted as outlined above under WARNINGS.

1. DIAGNOSTIC TESTING

For the patient with a suspected diagnosis of allergy to more than one antigen, initial skin testing should include the individual extracts. If a screening skin test with a mixture is used, a positive response should be followed by testing with the individual extracts to determine the degree of sensitivity to each and to guide in the selection of extracts and their concentration for immunotherapy if indicated. However, because a negative skin test with a mixture may not be indicative of the absence of allergy to one or more of the components due to their dilution, testing with individual extracts is more precise. False negative responses may occur if serum levels of antihistamines remain from prior medication administration (see CONTRAINDICATIONS). The use of a positive control is especially recommended for patients on prior medications which may decrease the histamine skin test response.

Scratch or Prick‑puncture Skin Testing:

Allergenic Extract concentrates may be used for scratch or prick‑puncture testing or scratch tests in 50% glycerin, 1:20 w/v or strongest available strength in 5 mL vials may be used. Prick‑puncture tests with concentrated extracts in patients highly sensitive to the specific antigen should yield distinctive wheals with diameters of greater than 5 mm and with much larger erythema reactions. Glycerinated histamine phosphate 5 mg/mL (1.8 mg/mL histamine base) or aqueous histamine phosphate 2.75 mg/mL (1 mg/mL histamine base; 1:1,000 W/V) may be used as a positive control.

Intradermal Skin Testing:

Extract for intradermal testing must be prepared by diluting the stock concentrate injection vials with sterile diluent (use normal or buffered saline, or normal saline with human serum albumin) or the appropriate dilutions may be purchased.

a. Patients with a negative scratch or prick‑puncture test:

Patients who do not react to a scratch or prick‑puncture test should be tested intradermally, using a 26 or 27 gauge 1/4 inch needle, with 0.02 to 0.05 mL of an appropriate extract dilution from 1/100 to 1/1000 of the concentrate. A negative test should be followed by a repeat test using a higher concentration until significant wheal and flare reaction sizes are attained or until the responses remain negative. As a negative control use the diluent or, in the case of extracts in 50% glycerin, use 0.5% to 1% glycerosaline solution. As a positive control, use glycerinated histamine phosphate diluted to 0.5 mg/mL (0.18 mg/mL histamine base) or aqueous histamine phosphate 0.275 mg/mL (0.1 mg/mL histamine base).

b. Patients tested only by the intradermal method:

Since highly reactive individuals may react intracutaneously at 1:1 million or even 1:10 million dilutions, any intradermal injection should be preceded by a puncture test and the dose adjusted accordingly. Other patients suspected of being moderately allergic should be tested with 0.02 to 0.05 mL of an appropriate extract dilution on the order of 1/10,000 to 1/100,000 of the concentrate. A negative test should be followed by repeat tests using progressively stronger ten‑fold concentrations until significant wheal and flare reaction sizes are attained, or until skin test responses with the higher concentrations remain negative. As a negative control, use the diluent or, in the case of extracts in 50% glycerin, use 0.5% to 1% glycerosaline solution. As a positive control, use glycerinated histamine phosphate diluted to 0.5 mg/mL (0.18 mg/mL histamine base) or aqueous histamine phosphate 0.275 mg/mL (0.1 mg/mL histamine base).

Skin tests are graded in terms of the wheal and erythema response noted at 15 to 20 minutes, and compared to the appropriate controls. Wheal and erythema sizes may be recorded by actual measurement.

2. IMMUNOTHERAPY

Immunotherapy is administered by subcutaneous injection. Dosage of Allergenic Extracts is individualized according to the patient's sensitivity, the clinical response, and tolerance to the extract administered during the phases of an injection regimen. The initial dose of the extract should be determined based on the puncture test reactivity. In patients who appear to be exquisitely sensitive by history and skin test, the initial dose of the extract should be 0.05 to 0.1 mL of a low concentration, such as dilution number 5 or 6 in below. Patients with lesser sensitivity may be started with 0.05 to 0.1 mL of the next higher concentration. The amount of Allergenic Extract is increased at each injection by no more than 50% of the previous amount, and the next increment is governed by the response to the last injection. Large local reactions which persist for longer than 24 hours are generally considered an indication for repeating the previous dose or reducing the dose at the next administration. Any evidence of systemic reaction is an indication for a reduction of 75% in the subsequent dose. The upper limits of dosage have not been established; however, doses larger than 0.2 mL of an extract in 50% glycerin may cause discomfort upon injection. The dosage of Allergenic Extract does not vary significantly with the allergic disease under treatment.

To prepare dilutions starting from a concentrate such as 1:10 W/V, 1:20 W/V, OR 20,000 PNU/mL, proceed as in Table 1 below. (Note: Add 0.5 mL of concentrate to 4.5 mL of sterile diluent and make additional dilutions in the same manner.)

TABLE 1

Ten-Fold Dilution Series *
*
There is no direct potency correlation across the table between PNUs and W/V.
DilutionExtractDiluentW/VW/VPNU/mL
0Concentrate1:101:2020,000
10.5 mL in dilution concentrate4.5 mL

1:100

1:2002,000
20.5 mL in dilution 14.5 mL1:1,0001:2,000200
30.5 mL in dilution 24.5 mL1:10,0001:20,00020
40.5 mL in dilution 34.5 mL1:100,0001:200,0002
50.5 mL in dilution 44.5 mL1:1,000,0001:2,000,0000.2
60.5 mL in dilution 54.5 mL1:10,000,0001:20,000,0000.0

Stock concentrate extracts containing up to 40,000 PNU/mL, or 1:10 W/V or other dilutions as requested by the physician are supplied in 5, 10, 30 and 50 mL in aqueous or 50% glycerin buffered saline. House dust extract is supplied in a 1:1 W/V concentrate, or a maximum of 10,000 PNU/mL. Extracts are also supplied in dropper vials for scratch or prick testing.

Allergenic Extracts should be stored at 2‑8°C and kept at this temperature range during office use. Refer to vial labels for expiration dates. Diluted extracts are inherently less stable than concentrates. Dilutions of glycerinated extracts which result in glycerin below 50% are also less stable. The more dilute extracts in aqueous diluents should be replenished daily. Potency of a particular dilution can be checked by skin test in comparison to a fresh dilution of the extract on an individual known to be allergic to the specific antigen.

  1. Lichtenstein LM, Ishizaka K, Norman PS, et al. IgE antibody measurements in ragweed hayfever: relationship to clinical severity and the results of immunotherapy. J Clin Invest 1973;52:474.
  2. Elgefors B, Julin A, Johansson SGO. Immunoglobulin E in bronchial asthma. Acta Allergol 1974;29:327.
  3. Norman PS. The clinical significance of IgE. Hosp Pract 1975;10:41‑49.
  4. Bryant DA, Burns MW, Lazarus L. The correlation between skin tests, bronchial provocation tests and the serum level of IgE specific for common allergens in patients with asthma. Clin Allergy 1975;5:145.
  5. Loeffler JA, Cawley LP, Moeder M. Serum IgE levels: correlation with skin test sensitivity. Ann Allergy 1973;31:331.
  6. Pepys J. Skin tests in diagnosis. In Gell PGH, Coombs RRA, Lachman PJ, eds. Clinical aspects of Immunology. Oxford: Blackwell Scientific Publications, 1975.
  7. Burrows B, et al. Respiratory disorders and allergy skin test reactions. Ann Allergy 1976;84:134.
  8. Implementation of Efficacy Review, Allergenic Extracts. Federal Register 1985;50:3082‑3288
  9. Levy DA, Lichenstein LM, Goldstein EO, Ishizaka K. Immunologic and cellular changes accompanying the therapy of pollen allergy. J Clin Invest 1973;50:360.
  10. Gurka G, Rocklin R. Immunologic responses during allergen-specific immunotherapy for respiratory allergy. Ann Allergy 1988;61:239-43.
  11. Zeiss CR Jr. Patient evaluation. In: Allergy and Clinical Immunology, Locky RF, ed. Garden City, N.Y.: Medical Examination Publishing 1976:616.
  12. Frankland AW, Augustin R. Prophylaxis of summer hay‑fever and asthma: a controlled trial comparing crude grass‑pollen extracts with the isolated main protein component. Lancet 1954;1:1055.
  13. Frankland AW, Augustin R. Grass pollen antigens effective in treatment. Clin Sci 1962;23:95.
  14. Rohr AS, Marshall NA, Saxon A: Successful immunotherapy for Triatoma protracta‑induced anaphylaxis. J Allergy Clin Immunol 1984;73:369‑75.
  15. Executive Committee, American Academy of Allergy and Immunology. The waiting period after allergen skin testing and immunotherapy (Position statement). J Allergy Clin Immunol 1990;85:526‑7.
  16. Greenberg MA, Kaufman CR, Gonzalez GE, Rosenblatt CD, Smith LJ, Summers RJ. Late and immediate systemic‑allergic reactions to inhalant allergen immunotherapy. J Allergy Clin Immunol 1986;77:865‑70.
  17. Ouellette JJ. Emergency management of the allergic reactions. Modern Medicine 1975;99.
  18. Anderson JA, et al. Personnel and equipment to treat systemic reactions caused by immunotherapy with allergenic extracts. J Allergy Clin Immunol 1986;77:271‑3.
  19. Sadan N, Rhyne MB, Mellits ED, et al. Immunotherapy of pollenosis in children: investigation of the immunologic basis of clinical improvement. N Eng J Med 1969;280:623.
  20. Johnstone DE. Value of hyposensitization therapy for perennial bronchial asthma in children. Pediatrics 1961;27:39.
  21. VanAsperin PP, Kemp AS, Mellis CM. Skin test reactivity and clinical allergen sensitivity in infancy. J Allergy Clin Immunol 1984;73:381‑6.
  22. Committee on Safety of Medicine. Desensitizing vaccines. Br Med J 1986;293:948.
  23. Lockey RF, Benedict LM, Turkeltaub PC, Bukantz SC. Fatalities from immunotherapy (IT) and skin testing (ST). J Allergy Clin Immunol 1987;79:660‑77.
  24. Norman PS, Van Metre TE Jr. The safety of allergenic immunotherapy. J Allergy Clin Immunol 1990;85:522‑5.

1600-2_Alternaria alternata_20000-pnu

1628-1_Aspergillus niger_1000-wv

5610-4_Candida albicans_20-wv

9641-5_Fusarium Mix_40-wv

LOOSE KERNEL SMUT 
sporisorium cruentum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5650
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5650-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5650-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:22840-5650-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
LOOSE SMUT, WHEAT 
ustilago tritici solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5653
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5653-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5653-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:22840-5653-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BARLEY LOOSE SMUT 
ustilago nuda solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5652
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO NUDA (UNII: 9Y53ZS6I82) (USTILAGO NUDA - UNII:9Y53ZS6I82) USTILAGO NUDA0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5652-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5652-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5652-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5624
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5624-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5624-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PAECILOMYCES VARIOTII 
paecilomyces variotii solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2607
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2607-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1621
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1621-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS STOLONIFER 
rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2624
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2624-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2624-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS STOLONIFER 
rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2625
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2625-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2634
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2634-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2634-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2677
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2677-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2646
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2646-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOPHYTON RUBRUM 
trichophyton rubrum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5640
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5640-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5640-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOTHECIUM ROSEUM 
trichothecium roseum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2652
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2652-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2652-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOTHECIUM ROSEUM 
trichothecium roseum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2653
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2653-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2653-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOTHECIUM ROSEUM 
trichothecium roseum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2655
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2655-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOTHECIUM ROSEUM 
trichothecium roseum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5641
Route of AdministrationSUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5641-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5641-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5641-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4NDC:22840-5641-330 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA ALTERNATA 
alternaria alternata solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5600
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5600-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:22840-5600-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5600-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2676
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2676-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA ALTERNATA 
alternaria alternata solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1600
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1600-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1600-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA ALTERNATA 
alternaria alternata solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1601
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1601-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1601-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FLAVUS 
aspergillus flavus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1610
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1610-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1610-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1615
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1615-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1615-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIGER 
aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1625
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1625-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1625-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CHAETOMIUM GLOBOSUM 
chaetomium globosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1648
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1648-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1648-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CHAETOMIUM GLOBOSUM 
chaetomium globosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1647
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1647-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1647-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CHAETOMIUM GLOBOSUM 
chaetomium globosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1650
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1650-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CHAETOMIUM GLOBOSUM 
chaetomium globosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1651
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1651-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9614
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.00025 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.00025 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.00025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.00025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9614-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9618
Route of AdministrationSUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM10000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER10000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA10000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9618-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9631
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0002 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.0002 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0002 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0002 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI0.0002 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9631-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DEMATIACEAE MIX 
alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9634
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.0083 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0083 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0083 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0083 g  in 1 mL
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.0083 g  in 1 mL
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI0.0083 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9634-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9649
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.00625 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.00625 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.00625 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.00625 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.00625 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.00625 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.00625 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.00625 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.00625 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.00625 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.00625 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.00625 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.00625 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.00625 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.00625 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.00625 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9649-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9649-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9652
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.003125 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.003125 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.003125 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.003125 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.003125 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.003125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.003125 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.003125 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.003125 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.003125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.003125 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.003125 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.003125 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.003125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.003125 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.003125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9652-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GRASS SMUT MIX 
ustilago cynodontis and sporisorium cruentum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9676
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.05 g  in 1 mL
SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9676-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DRECHSLERA SPICIFERA 
drechslera spicifera solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1664
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1664-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9636
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.025 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9636-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9636-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9637
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA20000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9637-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9637-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9638
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA10000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9638-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9639
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.0005 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9639-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MIX 
gibberella fujikuroi and fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9641
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.0125 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9641-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9641-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9641-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR MIX 
mucor circinelloides f. lusitanicus and mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9648
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.025 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9648-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9648-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9651
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI1250 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS1250 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA1250 [PNU]  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM1250 [PNU]  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA1250 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM1250 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM1250 [PNU]  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE1250 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS1250 [PNU]  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS1250 [PNU]  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM1250 [PNU]  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER1250 [PNU]  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES1250 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER1250 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS1250 [PNU]  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM1250 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9651-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9651-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9610
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER8000 [PNU]  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER8000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI8000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS8000 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS8000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9610-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9603
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.01 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.01 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.01 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.01 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9603-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9678
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER2500 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS2500 [PNU]  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS2500 [PNU]  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM2500 [PNU]  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES2500 [PNU]  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM2500 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER2500 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS2500 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI2500 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS2500 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA2500 [PNU]  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM2500 [PNU]  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA2500 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM2500 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM2500 [PNU]  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE2500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9678-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9680
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER10000 [PNU]  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9680-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9669
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0125 g  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9669-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9669-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9669-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1684
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1684-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9612
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0002 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0002 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0002 g  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.0002 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.0002 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9612-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9622
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.00033 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.00033 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.00033 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9622-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9673
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM13333.333 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS13333.333 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA13333.333 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9673-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9623
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.0166 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0166 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0166 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9623-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9623-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
AHH MOLD MIX 
alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9621
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.0166 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0166 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0166 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9621-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9621-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA/HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9624
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.025 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9624-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DRECHSLERA SPICIFERA 
drechslera spicifera solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1662
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1662-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9626
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.025 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9626-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9626-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1690
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1690-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR PLUMBEUS 
mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1696
Route of AdministrationSUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1696-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR PLUMBEUS 
mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5626
Route of AdministrationSUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5626-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5626-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIDULANS 
aspergillus nidulans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1622
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1622-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1622-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIDULANS 
aspergillus nidulans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2660
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2660-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
AUREOBASIDIUM PULLULANS 
aureobasidium pullulans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1630
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1630-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1635
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1635-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1635-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1636
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1636-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5608
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5608-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5608-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5608-55 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1617
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1617-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1617-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1618
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1618-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1618-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9650
Route of AdministrationSUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.0000625 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0000625 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0000625 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.0000625 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.0000625 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.0000625 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0000625 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.0000625 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0000625 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.0000625 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.0000625 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0000625 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.0000625 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0000625 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0000625 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.0000625 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9650-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9654
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.025 g  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.025 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9654-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9654-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GRASS SMUT MIX 
ustilago cynodontis and sporisorium cruentum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9671
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.05 g  in 1 mL
USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9671-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9671-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9671-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GRAIN SMUT MIX 
ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9675
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO NUDA (UNII: 9Y53ZS6I82) (USTILAGO NUDA - UNII:9Y53ZS6I82) USTILAGO NUDA0.0125 g  in 1 mL
USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.0125 g  in 1 mL
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.0125 g  in 1 mL
USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9675-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1641
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1641-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1641-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CORN SMUT 
ustilago maydis solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2664
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2664-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1643
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1643-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR MIX 
mucor circinelloides f. lusitanicus and mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9646
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.0005 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9646-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5631
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5631-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5631-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHODERMA HARZIANUM 
trichoderma harzianum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2640
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q) TRICHODERMA HARZIANUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2640-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2640-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9616
Route of AdministrationSUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM5000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER5000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA5000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM5000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9616-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9616-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9617
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.025 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.025 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9617-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9617-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA/HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9674
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS10000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9674-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9674-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ACREMONIUM STRICTUM 
acremonium strictum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5601
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5601-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5601-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9619
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.0125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9619-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MONILIA MIX 
candida albicans and neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9642
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS10000 [PNU]  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9642-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9642-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEW STOCK FUNGI MIX 
acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9653
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.003125 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.003125 g  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.003125 g  in 1 mL
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.003125 g  in 1 mL
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.003125 g  in 1 mL
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.003125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.003125 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.003125 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.003125 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.003125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.003125 g  in 1 mL
ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.003125 g  in 1 mL
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.003125 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.003125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.003125 g  in 1 mL
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.003125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9653-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9653-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9653-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GRAIN SMUT MIX 
ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9670
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO NUDA (UNII: 9Y53ZS6I82) (USTILAGO NUDA - UNII:9Y53ZS6I82) USTILAGO NUDA0.00625 g  in 1 mL
USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.00625 g  in 1 mL
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.00625 g  in 1 mL
USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI0.00625 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9670-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9670-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9670-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4NDC:22840-9670-330 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEUROSPORA INTERMEDIA 
neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2600
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2600-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2600-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEUROSPORA INTERMEDIA 
neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5627
Route of AdministrationSUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5627-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5627-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PAECILOMYCES VARIOTII 
paecilomyces variotii solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2605
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2605-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2605-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM DIGITATUM 
penicillium digitatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5630
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5630-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5630-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9630
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.01 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.01 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI0.01 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.01 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9630-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DEMATIACEAE MIX 
alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9635
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.0042 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0042 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0042 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0042 g  in 1 mL
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.0042 g  in 1 mL
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI0.0042 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9635-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9635-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIDULANS 
aspergillus nidulans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1623
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1623-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9629
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER4000 [PNU]  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS4000 [PNU]  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI4000 [PNU]  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS4000 [PNU]  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS4000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9629-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9629-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPICOCCUM NIGRUM 
epicoccum nigrum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2665
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2665-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2668
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2668-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2668-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5622
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5622-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5622-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5622-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR PLUMBEUS 
mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1694
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1694-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1694-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS ORYZAE 
rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5633
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5633-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
STEMPHYLIUM SOLANI 
stemphylium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2637
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2637-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2637-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
STEMPHYLIUM SOLANI 
stemphylium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2636
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2636-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
STEMPHYLIUM SOLANI 
stemphylium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5637
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5637-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:22840-5637-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2678
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2678-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5636
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5636-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5636-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
STEMPHYLIUM SOLANI 
stemphylium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2635
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2635-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2635-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
STEMPHYLIUM SOLANI 
stemphylium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2638
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2638-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2649
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2649-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. LUSITANICUS 
mucor circinelloides f. lusitanicus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2659
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2659-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPICOCCUM NIGRUM 
epicoccum nigrum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5616
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5616-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:22840-5616-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5616-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5617
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S) EPIDERMOPHYTON FLOCCOSUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5617-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5617-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5617-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4NDC:22840-5617-330 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MICROSPORUM CANIS 
microsporum canis solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5623
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICROSPORUM CANIS (UNII: N4F4RQ7BY7) (MICROSPORUM CANIS - UNII:N4F4RQ7BY7) MICROSPORUM CANIS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5623-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5623-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5623-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BERMUDA GRASS SMUT 
ustilago cynodontis solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5648
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5648-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5648-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5648-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MONILIFORME 
fusarium moniliforme solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1671
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1671-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1671-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS AMSTELODAMI 
aspergillus amstelodami solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1608
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1608-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIDULANS 
aspergillus nidulans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5605
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5605-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIGER 
aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1626
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1626-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIGER 
aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5606
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5606-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5606-55 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1644
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1644-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1644-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPICOCCUM NIGRUM 
epicoccum nigrum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1666
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1666-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIGER 
aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1628
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1628-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1633
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1633-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1633-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DRECHSLERA SPICIFERA 
drechslera spicifera solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5615
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5615-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5615-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5615-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM SOLANI 
fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1676
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1676-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PHOMA BETAE 
phoma betae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2618
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2618-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM SOLANI 
fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5619
Route of AdministrationSUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5619-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5619-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1681
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1681-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1681-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1682
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1682-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1691
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1691-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1691-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BOTRYTIS CINEREA 
botrytis cinerea solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2662
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2662-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM HERBARUM 
cladosporium herbarum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1653
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1653-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1653-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM HERBARUM 
cladosporium herbarum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1654
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1654-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1654-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM HERBARUM 
cladosporium herbarum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1656
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1656-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA ALTERNATA 
alternaria alternata solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1605
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1605-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS AMSTELODAMI 
aspergillus amstelodami solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1609
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1609-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BOTRYTIS CINEREA 
botrytis cinerea solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1639
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1639-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MONILIFORME 
fusarium moniliforme solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1670
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1670-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1670-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1619
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.002 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1619-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2615
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2615-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PHOMA BETAE 
phoma betae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5632
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5632-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5632-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:22840-5632-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS ORYZAE 
rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2619
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2619-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9627
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.02 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.02 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI0.02 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.02 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.02 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9627-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9627-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA ALTERNATA 
alternaria alternata solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1604
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1604-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ACREMONIUM STRICTUM 
acremonium strictum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1606
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1606-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS STOLONIFER 
rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2623
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2623-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2623-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. LUSITANICUS 
mucor circinelloides f. lusitanicus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2671
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2671-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOTHECIUM ROSEUM 
trichothecium roseum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2654
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2654-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2654-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOTHECIUM ROSEUM 
trichothecium roseum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2656
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2656-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MYCOGONE PERNICIOSA 
mycogone perniciosa solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5642
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U) HYPOMYCES PERNICIOSUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5642-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5642-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5642-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9609
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER2000 [PNU]  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER2000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI2000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS2000 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS2000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9609-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9609-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1632
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1632-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1632-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9656
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM5000 [PNU]  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI5000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM5000 [PNU]  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI5000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9656-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9655
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM10000 [PNU]  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI10000 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM10000 [PNU]  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9655-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9655-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9657
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.0125 g  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0125 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9657-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9657-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9679
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM2500 [PNU]  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI2500 [PNU]  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM2500 [PNU]  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI2500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9679-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1667
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S) EPIDERMOPHYTON FLOCCOSUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1667-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1667-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1669
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S) EPIDERMOPHYTON FLOCCOSUM1000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1669-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1659
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1659-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DRECHSLERA SPICIFERA 
drechslera spicifera solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1661
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1661-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1661-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PAECILOMYCES VARIOTII 
paecilomyces variotii solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2606
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2606-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2606-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHODERMA HARZIANUM 
trichoderma harzianum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5638
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q) TRICHODERMA HARZIANUM0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5638-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5638-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5638-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2645
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2645-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2645-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MONILIFORME 
fusarium moniliforme solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1673
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1673-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM SOLANI 
fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1678
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1678-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9601
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM4000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER4000 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS4000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA4000 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM4000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9601-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9601-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MONILIFORME 
fusarium moniliforme solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1674
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1674-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM SOLANI 
fusarium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1677
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1677-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GEOTRICHUM CANDIDUM 
geotrichum candidum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1680
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1680-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5621
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5621-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5621-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5621-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR PLUMBEUS 
mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1698
Route of AdministrationSUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1698-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEUROSPORA INTERMEDIA 
neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2601
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2601-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PAECILOMYCES VARIOTII 
paecilomyces variotii solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2609
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2609-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2609-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PAECILOMYCES VARIOTII 
paecilomyces variotii solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5629
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5629-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5629-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5629-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2614
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2614-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2614-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PHOMA BETAE 
phoma betae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2674
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2674-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS NIGER 
aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1627
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1627-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CORN SMUT 
ustilago maydis solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5649
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5649-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5649-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:22840-5649-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
OAT SMUT 
ustilago avenae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5651
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5651-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5651-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:22840-5651-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9602
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM8000 [PNU]  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER8000 [PNU]  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS8000 [PNU]  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA8000 [PNU]  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM8000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9602-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9602-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9604
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0002 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0002 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0002 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0002 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.0002 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9604-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9606
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.01 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.01 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.01 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.01 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9606-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9606-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9606-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9608
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER4000 [PNU]  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER4000 [PNU]  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI4000 [PNU]  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS4000 [PNU]  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS4000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9608-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9608-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ACREMONIUM STRICTUM 
acremonium strictum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2679
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2679-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BOTRYTIS CINEREA 
botrytis cinerea solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5609
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5609-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5609-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1646
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1646-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS STOLONIFER 
rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2627
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2627-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS STOLONIFER 
rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5634
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5634-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5634-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2628
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z) RHODOTORULA MUCILAGINOSA0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2628-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5610
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5610-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5610-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM HERBARUM 
cladosporium herbarum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5613
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5613-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:22840-5613-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 1 
alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9600
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.02 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.02 g  in 1 mL
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.02 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.02 g  in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.02 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9600-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9600-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1683
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1683-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9660
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.0125 g  in 1 mL
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0125 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9660-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9660-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9660-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM MIX 
penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9659
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.00025 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.00025 g  in 1 mL
PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.00025 g  in 1 mL
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.00025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9659-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PHYCOMYCETES MIX 
mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9661
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.025 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9661-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PHYCOMYCETES MIX 
mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9662
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.0005 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9662-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PHYCOMYCETES MIX 
mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9664
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.0125 g  in 1 mL
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9664-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9664-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9664-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4NDC:22840-9664-330 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9665
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.025 g  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9665-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9665-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9666
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER20000 [PNU]  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9666-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS MIX 
rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9668
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0005 g  in 1 mL
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9668-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FLAVUS 
aspergillus flavus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1612
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1612-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2661
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2661-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
TRICHODERMA HARZIANUM 
trichoderma harzianum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2642
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (TRICHODERMA HARZIANUM - UNII:CA33Q4013Q) TRICHODERMA HARZIANUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2642-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. LUSITANICUS 
mucor circinelloides f. lusitanicus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5625
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5625-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CHAETOMIUM GLOBOSUM 
chaetomium globosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5612
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5612-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5612-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2663
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2663-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5614
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5614-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5614-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5614-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2669
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2669-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA/HORMODENDRUM MIX 
alternaria alternata and aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9625
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0005 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9625-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MONILIA MIX 
candida albicans and neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9643
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS500 [PNU]  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA500 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9643-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FLAVUS 
aspergillus flavus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5603
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.025 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5603-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5603-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5603-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
BIPOLARIS SOROKINIANA 
bipolaris sorokiniana solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1634
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1634-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1634-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CLADOSPORIUM HERBARUM 
cladosporium herbarum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1657
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1657-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1640
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1640-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
CANDIDA ALBICANS 
candida albicans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1642
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1642-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS AMSTELODAMI 
aspergillus amstelodami solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5602
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5602-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5602-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5602-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM DIGITATUM 
penicillium digitatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2610
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2610-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2610-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR MIX 
mucor circinelloides f. lusitanicus and mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9672
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (MUCOR CIRCINELLOIDES F. LUSITANICUS - UNII:0J0X819B3C) MUCOR CIRCINELLOIDES F. LUSITANICUS0.05 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9672-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9607
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.01 g  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.01 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.01 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.01 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9607-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9607-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9628
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER8000 [PNU]  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS8000 [PNU]  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI8000 [PNU]  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS8000 [PNU]  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS8000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9628-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9628-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS MIX 
aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9633
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.01 g  in 1 mL
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.01 g  in 1 mL
EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (EUROTIUM AMSTELODAMI - UNII:D932NLL87Z) EUROTIUM AMSTELODAMI0.01 g  in 1 mL
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.01 g  in 1 mL
ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.01 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9633-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9633-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9633-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MONILIA MIX 
candida albicans and neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9644
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.0005 g  in 1 mL
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.0005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9644-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1616
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1616-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FLAVUS 
aspergillus flavus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1614
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOL (UNII: 339NCG44TV)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1614-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ASPERGILLUS FUMIGATUS 
aspergillus fumigatus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5604
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5604-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5604-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5604-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
AUREOBASIDIUM PULLULANS 
aureobasidium pullulans solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5607
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.025 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5607-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:22840-5607-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5607-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 3 
alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9620
Route of AdministrationINTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM0.0125 g  in 1 mL
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0125 g  in 1 mL
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0125 g  in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0125 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9620-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9620-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9620-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MOLD MIX 2 
aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-9613
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.005 g  in 1 mL
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.005 g  in 1 mL
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.005 g  in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.005 g  in 1 mL
MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.005 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-9613-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-9613-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-9613-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
DRECHSLERA SPICIFERA 
drechslera spicifera solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1660
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1660-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1660-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
EPIDERMOPHYTON FLOCCOSUM 
epidermophyton floccosum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2666
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S) EPIDERMOPHYTON FLOCCOSUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2666-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1692
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1692-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 
mucor circinelloides f. circinelloides solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2670
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES - UNII:48Z8OUT98B) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2670-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEUROSPORA INTERMEDIA 
neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1699
Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1699-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1699-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
NEUROSPORA INTERMEDIA 
neurospora intermedia solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2602
Route of AdministrationSUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2602-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PAECILOMYCES VARIOTII 
paecilomyces variotii solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2673
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2673-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2616
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2616-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MONILIFORME 
fusarium moniliforme solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1672
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1672-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GEOTRICHUM CANDIDUM 
geotrichum candidum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5620
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5620-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5620-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5620-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) 
penicillium chrysogenum (notatum) solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2612
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2612-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHIZOPUS ORYZAE 
rhizopus oryzae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2621
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2621-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
RHODOTORULA MUCILAGINOSA 
rhodotorula mucilaginosa solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2630
Route of AdministrationSUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (RHODOTORULA MUCILAGINOSA - UNII:62TY3X4N9Z) RHODOTORULA MUCILAGINOSA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2630-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-2630-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
SACCHAROMYCES CEREVISIAE 
saccharomyces cerevisiae solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2633
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2633-15 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
ALTERNARIA ALTERNATA 
alternaria alternata solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1602
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1602-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1602-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
FUSARIUM MONILIFORME 
fusarium moniliforme solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-5618
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (GIBBERELLA FUJIKUROI - UNII:815V716OR2) GIBBERELLA FUJIKUROI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-5618-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-5618-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
3NDC:22840-5618-55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GEOTRICHUM CANDIDUM 
geotrichum candidum solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-2667
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-2667-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1685
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE20000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1685-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1685-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
GLIOCLADIUM VIRIDE 
gliocladium viride solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1686
Route of AdministrationPERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (GLIOCLADIUM VIRIDE - UNII:8Z8C642TPL) GLIOCLADIUM VIRIDE40000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1686-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
HELMINTHOSPORIUM SOLANI 
helminthosporium solani solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1689
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22840-1689-210 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
2NDC:22840-1689-450 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10183309/15/1981
MUCOR PLUMBEUS 
mucor plumbeus solution
Product Information
Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:22840-1695
Route of AdministrationINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS