Label: SOLIDAGO CANADENSIS POLLEN- goldenrod injection, solution
JUNIPERUS CALIFORNICA POLLEN- juniper western injection, solution
CHENOPODIUM ALBUM POLLEN- lambs quarters injection, solution
CHENOPODIUM AMBROSIOIDES POLLEN- mexican tea injection, solution
QUERCUS AGRIFOLIA POLLEN (oak california live coast) injection ......./strong> JUGLANS REGIA POLLEN (walnut english pollen) injection, solution AMARANTHUS TUBERCULATUS POLLEN (water hemp) injection, solution TRITICUM AESTIVUM POLLEN (wheat pollen) injection, solution SALIX NIGRA POLLEN (willow black) injection, solution ARTEMISIA ANNUA POLLEN- wormwood common annual injection, solution [ALK-Abello, Inc.]
JUGLANS REGIA POLLEN- walnut english pollen injection, solution
AMARANTHUS TUBERCULATUS POLLEN- water hemp injection, solution
TRITICUM AESTIVUM POLLEN- wheat pollen injection, solution
SALIX NIGRA POLLEN- willow black injection, solution
ARTEMISIA ANNUA POLLEN- wormwood common annual injection, solution

  • NDC Code(s): 0268-0001-10, 0268-0002-50, 0268-0003-10, 0268-0004-10, view more
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  • Packager: ALK-Abello, Inc.
  • Category: NON-STANDARDIZED ALLERGENIC LABEL
  • DEA Schedule: None
  • Marketing Status: Biologic Licensing Application

Drug Label Information

Updated November 12, 2021

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    DIRECTIONS FOR USE OF

    THERAPEUTIC ALLERGENIC EXTRACTS

  • BOXED WARNING (What is this?)

    WARNING

    This 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.

    Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician’s office if reaction symptoms occur. As with all allergenic extracts, severe systemic reactions may occur. In certain individuals, these reactions may rarely result in death. Patients should be observed for 20 to 30 minutes following treatment, and emergency measures, as well as personnel trained in their use, should be immediately available in the event of a life-threatening reaction. Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk. Adverse events are to be reported to Med Watch (1-800-FDA-1088), Adverse Event Reporting , Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20852-9787.

    This product should not be injected intravenously. Deep subcutaneous routes have proven to be safe. Patients receiving beta-blockers may not be responsive to epinephrine or inhaled bronchodilators. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require theophylline, oxygen, intubation and the use of life support systems. Parenteral fluid and/or plasma expanders may be utilized for the treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously.

    Refer to WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS sections below.

  • SPL UNCLASSIFIED SECTION

    Port Washington, NY 11050

    U.S. Government License No. 1256

  • DESCRIPTION

    Sterile therapeutic extracts are supplied in either Phenol Saline Diluent or in Diluent containing Glycerin 50% (v/v) for subcutaneous injection. Inactive ingredients may include: Sodium Chloride for isotonicity, Glycerin, and Sodium Bicarbonate as buffering agents. These products are compounded and diluted on a w/v or PNU basis. Pollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and, after final packaging, they are tested for sterility and safety. Molds are individually extracted from pure powdered inactivated mold source material extracted in phenol preserved saline. Mold extracts are filtered aseptically and after final packaging are tested for sterility and safety. Molds are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously.

    Miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline, filtered aseptically and after final packaging are tested for sterility and safety.

  • CLINICAL PHARMACOLOGY

    The treatment consists of the subcutaneous injection of gradually increasing doses of the allergens to which the patient is allergic. It has been demonstrated that this method of treatment induces an increased tolerance to the allergens responsible for the symptoms on subsequent exposure. The exact relationships between allergen, skin-sensitizing antibody (IgE) and the blocking antibody (IgG) have not been precisely established. Clinically confirmed immunological studies have adduced evidence of the efficacy of hyposensitization therapy.

    Numerous controlled studies have demonstrated the clinical efficacy of immunotherapy with cat, dust mites and some pollen extracts. Nevertheless, responses are variable, and in a few studies patients reported no appreciable benefit.

    Extracts containing Short Ragweed pollen bear a labeled potency declaration in terms of Antigen E content. Numerous studies have confirmed Antigen E (AgE) as the major antigen associated with Short Ragweed pollinosis.1 Therefore, it is essential that the physician be aware of AgE content of allergenic extract administered for hyposensitization therapy.

    Some studies have indicated that for most patients a cumulative Antigen E dosage of less than 0.1 unit is not immunizing (sufficient to stimulate specific IgG antibodies).2 This, however, does not suggest that 0.1 unit is a maximum tolerated dose. Most moderately sensitive patients may tolerate a dosage of ten to fifty times greater. If results with this product are unsatisfactory with exquisitely sensitive patients who cannot tolerate an immunizing dose, the physician should consider alternative therapy.

    One well-controlled study demonstrated that standard immunotherapy (gradually increasing doses of antigen given subcutaneously to a maximum tolerated peak dose) using crude ragweed extract of known Antigen E potency, was significantly superior to placebo and low dose immunotherapy (0.1 units AgE cumulative dose) in amelioration of symptoms associated with ragweed hay fever. These patients received a cumulative dose of 18-350 units Antigen E (median = 84.9 units). The maximum single dose ranged from 3.7 to 46.8 units (median = 11.1 units) prior to the ragweed hay fever season.10

    Patients for this study were sensitive to Ragweed Antigen E, as determined by intradermal skin testing at a dose of 0.01 units AgE/mL. A series of 24 weekly injections were administered. Forty-seven percent of the patients experienced at least one systemic reaction with an average of 1.2 systemic reactions per patient. None of the patients were able to achieve the expected maximum dose (90 units of Antigen E) in the 24 weekly injection dosage schedule.

  • INDICATIONS AND USAGE

    Hyposensitization (injection) therapy is a treatment for patients exhibiting allergic reactions to seasonal pollens, dust, molds, animal danders, various other inhalants, and in situations where the offending allergen cannot be avoided.

    Prior to initiation of therapy, the clinical sensitivity should be established by careful evaluation of the patient’s history confirmed by diagnostic skin testing. Hyposensitization should not be prescribed for sensitivities to allergens which can easily be avoided.

  • CONTRAINDICATIONS

    A patient should not be immunized with preparations of allergens to which the patient has not demonstrated symptoms, IgE antibodies, positive skin tests, or properly controlled challenge testing. In most cases, immunotherapy is not indicated for those allergens that can be eliminated or minimized by environmental control.

    Patients on beta-blockers are not candidates for immunotherapy, as they can be non-responsive to beta-agonists that may be required to reverse a systemic reaction (also see WARNINGS AND ADVERSE REACTIONS).

    In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indication of immunotherapy must be weighed carefully against the risk of temporarily aggravating the symptoms by the injection itself.

    Also, there is some evidence, although inconclusive, that routine immunizations may exacerbate autoimmune diseases.3,4,5 Hyposensitization should be given cautiously to patients with this predisposition. Patients with severe cardiorespiratory symptoms are at an additional risk during a systemic reaction. The physician must weigh risk to benefit in these cases.

  • WARNINGS

    Patients should always be observed for at least 20-30 minutes after any injection. In the event of a marked systemic reaction, application of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of Epinephrine Injection (1:1,000) is recommended. Maximal recommended dose for children between 2 and 12 years is 0.5 mL. The tourniquet is then gradually released at 15 minute intervals. Patients under treatment with beta-blockers may be refractory to the usual dose of epinephrine.

    Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In cases of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reaction unresponsive to the above may require cardiopulmonary resuscitation.

    DO NOT GIVE INTRAVENOUSLY

    After inserting the needle, but before injecting the dose, pull plunger of the syringe slightly. If blood returns in the syringe, discard the syringe and contents and repeat injection at another site.

    Bulk concentrated extracts must be diluted for initial therapy.

    Withhold allergenic extracts temporarily or reduce the dose in patients with any one of the following conditions:

    - Severe rhinitis or asthma symptoms;

    - Infection or flu accompanied by fever;

    - Exposure to excessive amounts of clinically relevant allergen prior to therapy.

    Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk. See PRECAUTIONS AND ADVERSE REACTIONS.

    TRANSFER OF PATIENTS

    From pyridine extracted alum complexed allergenic extracts to aqueous extracts and glycerinated: In order to avoid untoward reaction, it is recommended that therapy be initiated as though patients were previously untreated. The first dose should be related to the patient’s sensitivity, determined by history and confirmed by skin testing.

    From unstandardized aqueous extracts to standardized aqueous extracts and glycerinated: The physician should establish the potency relationship, perhaps by comparative skin testing at equal concentration, prior to injecting the first standardized dose.

    From aqueous alum precipitated or modified extracts to aqueous extracts and glycerinated: Since this subject has not been studied, it is recommended that therapy be initiated as if the patient were not previously treated.

  • PRECAUTIONS

    INFORMATION TO PATIENTS:

    Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to injection including any late reactions from previous administration. Patients should be instructed to remain in the office for 20 to 30 minutes after injection to monitor for adverse reactions. Also, see ADVERSE REACTIONS and WARNINGS Sections.

    If the protective action of allergenic extract injections is considered essential for the patient’s welfare, appropriate symptomatic therapy with antihistaminic, adrenergic or other drugs might be needed either prior to or in conjunction with the allergenic extract injections.

    GENERAL:

    1. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration may be useful in unstable asthmatic to reduce the chances of exacerbation of the patient’s asthma.
    2. Store allergenic extracts between 2° and 8°C at all times, even during use.
    3. Injections are to be given subcutaneously with the usual sterile precautions using a tuberculin syringe.
    4. Care must be taken to avoid injecting into a blood vessel. Pull gently on syringe plunger to determine if a blood vessel has been entered (See WARNINGS).
    5. Allergenic extracts slowly become less potent with age. During the course of treatment, it may be necessary to continue therapy with a vial of extract bearing a later expiration date. The initial dose of the extract bearing the later expiration date should be lowered to a safe, non-reaction eliciting level which can be confirmed by comparative skin testing using end-point titration.
    6. Use standard aseptic precautions when making dilutions. The first dose of the new extract should be reduced to at least 25% of the amount of the dosage from the previous extract.
    7. Extracts in 50% glycerin can cause discomfort at the site of the injection.

    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 can affect reproduction capacity.

    Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother. However, on the basis of histamine’s known ability to contract uterine muscle, the release of significant amounts of histamine from allergen exposure or hyposensitization overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.

    PEDIATRIC USE:

    Children can receive the same dose as adults, however, to minimize the discomfort associated with dose volume it may be advisable to reduce the volume of the dose by one-half and administer the injection at two different sites.

    NURSING MOTHERS:

    It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

    CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY:

    Studies in animals have not been performed.

    DRUG INTERACTIONS:

    Drugs can interfere with the performance of skin tests.6

    Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine), and can be as long as 40 days (astemizole).

    Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.

    Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.

    Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.

    Beta Blocking Agents: Propranolol can significantly increase skin test reactivity (See WARNINGS).

    Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.

  • ADVERSE REACTIONS

    Anaphylaxis and deaths following the injection of mite and other extracts have been reported by The British Committee on Safety in Medicine.7 Fatalities from immunotherapy in the United States since 1945 have been extensively reviewed by Lockey, R. F., et al8 and more recently by Reid, M. ⁠J. et al.9

    With careful attention to dosage and administration, such reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and OVERDOSE could result in anaphylactic symptoms. Therefore, it is imperative that physicians administering allergenic extracts understand and be prepared for the treatment of severe reactions.

    Local: Reactions at the site of injection may be immediate or delayed. Immediate wheal and erythema reactions are ordinarily of little consequence; but if very large, may be the first manifestation of a systemic reaction. If large local reactions occur, the patient should be observed for systemic symptoms for which treatment is outlined below.

    Delayed reactions start several hours after injection with local edema, erythema, itching or pain. They are usually at their peak at 24 hours and usually require no treatment. Antihistamine drugs may be administered orally.

    The next therapeutic dose should be reduced to the dose which did not elicit a reaction, and subsequent doses increased more slowly; i.e., use of intermediate dilutions.

    Systemic: Systemic reactions are characterized by one or more of the following symptoms: Sneezing, mild to severe generalized urticaria, itching other than at the injection site, extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, tachycardia, lacrimation, marked perspiration, cough, hypotension, syncope and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 to 30 minutes after any injection. Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction, unresponsive to bronchodilator, may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.2 mL to 1 mL of Epinephrine Injection (1:1,000) are recommended. Maximal recommended dose for children under 2 years of age is 0.3 mL. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet should not be left in place without loosening for 90 seconds every 15 minutes.

    The next therapeutic injection of extract should be reduced to the dose which did not elicit a reaction, and subsequent doses increased more slowly; i.e., use of intermediate dilutions.

  • OVERDOSAGE

    Signs and symptoms of overdose are typically local and systemic reactions. For a description and management of overdose reactions, refer to “Adverse Reaction” section above.

  • DOSAGE AND ADMINISTRATION

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    When diluting bulk extracts, use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly, 10 fold dilutions are used to achieve a desired concentration for initiation and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of diluent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration.

    Starting dose for immunotherapy is related directly to a patient’s sensitivity as determined by carefully executed skin testing. Degree of sensitivity can be established by determination of D50.11 A general rule is to begin at 1/10 of the dose that produces sum of erythema of 50 mm (approximately a 2+ positive skin test reaction).

    For example, if a patient exhibits a 2+ intradermal reaction to 1 AU/mL, the first dose should be no higher than 0.05 mL of 0.1 AU/mL. Dosage may be increased by 0.05 mL each time until 0.5 mL is reached, at which time the next 10-fold more concentrated dilution can be used, beginning with 0.05 mL, if no untoward reaction is observed.

    Interval between doses in the early stages of immunotherapy is no more than once to twice a week, and may gradually be increased to once every two weeks. Generally, maintenance injections may be given as infrequently as once every two weeks to once a month.

    Injections are given subcutaneously, preferably in the arm. It is advantageous to give injections in alternate arms and routinely in the same area. In some patients, a local tolerance to the allergen may develop thus preventing a possible severe local reaction.

    Formal stability studies for diluted and undiluted forms of unstandardized extracts have not been performed; therefore, it is recommended that minimal amounts of the concentrate be diluted so that the diluted product is used up within a relatively short period of time; i.e., preferably not more than four weeks.

    PRE-SEASONAL METHOD OF TREATMENT

    Treatment of hay fever by the pre-seasonal method should be started 6-10 weeks prior to the usual onset of symptoms. Therapy should be started early enough to permit a graduated series of doses at 2-7 day intervals. It is recommended that the larger doses be spaced 5-7 days apart.

    Some physicians continue therapy into or through the season by repeating a reduced or MAINTENANCE dose at weekly or biweekly intervals. If during the season, hay fever symptoms develop, relief may be provided by giving supplemental treatment. If the last dose was well-tolerated and not more than 2 weeks has elapsed since it was given, this dose may be given again and repeated every 4 to 7 days.

    PERENNIAL TREATMENT

    The patient’s tolerance to the offending pollen or pollens is first established by the injection of a series of graduated doses as outlined in the PRE-SEASONAL METHOD, not necessarily given pre-seasonally, since perennial therapy may be begun at any time. After completion of the ascending series of injections, from 1/4 to 1/2 of the highest well-tolerated dose is continued at 2 to 3 week intervals throughout the year. Shortly before the usual onset of symptoms (4 to 5 weeks prior to the season) the interval between injections is shortened and the dosage is gradually increased, according to the Pre-Seasonal schedule, until maximum well-tolerated dose is again attained. This top dose should be reached just before the usual onset of symptoms at which time the treatment is discontinued. If patient’s symptoms persist, therapy may be continued at a reduced dosage level, usually 1/4 to 1/2 of the top dose.

    DOSAGE ADJUSTMENTS

    For Products Containing Short Ragweed.

    In transferring patients from unstandardized to standardized product, the physician should establish the potency relationships, perhaps by comparative skin testing, prior to injecting the first standardized dose.

    AgE is important in adjusting dosage of Short Ragweed extracts to accurately transfer a patient from older extracts to fresher material. In such cases, the dosage of AgE should be considered in addition to the W/V dilution or protein nitrogen units. Antigen E concentration continuously declines in Short Ragweed Pollen extracts at a rate that varies with the formulation of the product. Aqueous extracts retain Antigen E potency less effectively than glycerin 50% (v/v) extracts. These differences are reflected in the expiration date declared on the vial. The continuous decline should be considered. Also, where ragweed is a component of an allergen mixture, clinical response to the other components must be considered in adjustment of dosage based on AgE content alone. The usual course of immunotherapy is three to five years.

    Caution: A small percent of individuals allergic to Short Ragweed are more sensitive to minor antigens such as Ra3 Ra5 than AgE. There is no correlation between the amount of these antigens and either AgE or PNU content.

    NOTE: For extracts of Short Ragweed or equal part mixture of Short and Tall Ragweed refer to AgE dosage schedule. The AgE content for those products is indicated on the vial label. The physician may use the formula below to determine the AgE dosage for each injection.

    AgE dosage can be monitored by using the following formula:

    W/V compounded products:

    Labeled AgE X Dose (mL) = dose in AgE

    PNU compounded products:

    Labeled AgE/mL X dose in PNU = dose in AgE

    Labeled PNU/mL

  • HOW SUPPLIED

    1. Concentrate in multiple dose vials:
    2. Sterile Diluent for Allergenic Extracts (Phenol Saline) is supplied in vials of 4.5 mL, 9.0 mL, 30 mL and 100 mL.

    10 mL and 50 mL, single antigens or specified mixtures, potency expressed in PNU/mL (up to and including 100,000 PNU/mL) or W/V (up to and including 1:10 W/V), aqueous or in 50% glycerin, to be diluted prior to use. 1:10 w/v short ragweed extracts contain ≥ 300 units/mL of AgE.

    STORAGE: To maintain stability of allergenic extracts, proper storage conditions are essential. Bulk concentrates and diluted extracts are to be stored at 2° to 8° C even during use. Bulk or diluted extracts are not to be frozen. Do not use after the expiration date shown on the vial label.

  • REFERENCES

    1. Norman, P.S. et al: Immunotherapy of hayfever with ragweed antigen E. Comparisons with whole pollen extract and placebo. J. Allergy 42:93, 1968.
    2. Van Metre, T.E. et al: A controlled study of the effectiveness of the Rinkel method of immunotherapy for ragweed pollen hayfever. J. Allergy Clin. Immunol. 65:288, 1980.
    3. Umetsu, D.T. et al: Serum sickness triggered by anaphylaxis: a complication of immunotherapy. J. Allergy Clin. Immunol. 76:713, 1985.
    4. Phannphak, P. and Kohler, P.F.: Onset of polyarteritis nodosa during allergic hyposenitization treatment. Am. J. Med. 68:479, 1980.
    5. Kohler, P.F.: Immune complexes and allergic disease. In: Middleton et al: Allergy Principles and Practice 3rd Ed. St. Louis: CV Mosby, 1988:167.
    6. Bousquet, J.: In vivo methods for the study of allergy: skin test, techniques, and interpretation. In: Middleton et al: Allergy Principles and Practice 3rd Ed. St. Louis: CV Mosby, 1988:167.
    7. Committee on the Safety of Medicines. CSM update: desensitising vaccines. Brit Med. J. 293:948,1986.
    8. Lockey, R.F. et al: Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol. 79:660, 1987.
    9. Reid, M.J. et al: Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin. Immunol.;92:6, 1993.
    10. Van Metre, T.E. et al: A controlled study of the effectiveness of the Rinkel method and the current standard method of immunotherapy for ragweed pollen hayfever. J. Allergy Clin. Immunol. 66:500, 1980.
    11. Turkeltaub, P.C., Rastogi, S.C., Baer, H., et al: A standardized quantitative skin-test assay of allergen potency and stability: studies on the allergen dose-response curve and effect of wheal, erythema, and patient selection on assay results, J. Allergy Clin. Immunol. 70:343, 1982.

    Revised April 2017                                                       158M      

    © ALK-Abelló, Inc. 

    Distributed in Canada by:

    ALK-Abelló Pharmaceuticals, Inc.

    #35-151 Brunel Road

    Mississauga, Ontario

    Canada L4Z 2H6

  • PRINCIPAL DISPLAY PANEL

    ALLERGENIC EXTRACT
    mL sterile multiple dose vial

    PRINCIPAL DISPLAY PANEL
ALLERGENIC EXTRACT
mL sterile multiple dose vial

  • INGREDIENTS AND APPEARANCE
    SOLIDAGO CANADENSIS POLLEN 
    goldenrod injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1194
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (SOLIDAGO CANADENSIS POLLEN - UNII:644CZ16IR5) SOLIDAGO CANADENSIS POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1194-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    JUNIPERUS CALIFORNICA POLLEN 
    juniper western injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1609
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L) JUNIPERUS CALIFORNICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1609-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    CHENOPODIUM ALBUM POLLEN 
    lambs quarters injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1610
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1610-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CHENOPODIUM AMBROSIOIDES POLLEN 
    mexican tea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1611
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (CHENOPODIUM AMBROSIOIDES POLLEN - UNII:WIB701MW2H) CHENOPODIUM AMBROSIOIDES POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1611-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1611-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    QUERCUS AGRIFOLIA POLLEN 
    oak california live coast injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1612
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7) QUERCUS AGRIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1612-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    QUERCUS ALBA POLLEN 
    oak white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1331
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1331-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    CARYA ILLINOINENSIS POLLEN 
    pecan pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1356
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1356-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CARYA ILLINOINENSIS POLLEN 
    pecan pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1357
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1357-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PLANTAGO LANCEOLATA POLLEN 
    plantain english injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1398
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1398-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PYRETHRUM CINERARIIFOLIUM 
    pyrethrum cinerariifolium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0645
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TANACETUM CINERARIIFOLIUM FLOWER (UNII: CGF76TP7X6) (TANACETUM CINERARIIFOLIUM FLOWER - UNII:CGF76TP7X6) TANACETUM CINERARIIFOLIUM FLOWER0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0645-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PYRETHRUM CINERARIIFOLIUM 
    pyrethrum cinerariifolium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0646
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TANACETUM CINERARIIFOLIUM FLOWER (UNII: CGF76TP7X6) (TANACETUM CINERARIIFOLIUM FLOWER - UNII:CGF76TP7X6) TANACETUM CINERARIIFOLIUM FLOWER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0646-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375302/23/1998
    AMARANTHUS RETROFLEXUS POLLEN 
    pigweed rough redroot injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1615
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1615-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375302/23/1998
    IVA ANNUA VAR ANNUA POLLEN 
    marshelder rough injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1266
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1266-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MELALEUCA QUINQUENERVIA POLLEN 
    melaleuca pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1273
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1273-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1273-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MELALEUCA QUINQUENERVIA POLLEN 
    melaleuca pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1274
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1274-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1274-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MELALEUCA QUINQUENERVIA POLLEN 
    melaleuca pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1275
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1275-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MELALEUCA QUINQUENERVIA POLLEN 
    melaleuca pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1276
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1276-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PROSOPIS JULIFLORA POLLEN 
    mesquite injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1279
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1279-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1279-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PROSOPIS JULIFLORA POLLEN 
    mesquite injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1280
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1280-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1280-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PROSOPIS JULIFLORA POLLEN 
    mesquite injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1281
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1281-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    CHENOPODIUM AMBROSIOIDES POLLEN 
    mexican tea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1284
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (CHENOPODIUM AMBROSIOIDES POLLEN - UNII:WIB701MW2H) CHENOPODIUM AMBROSIOIDES POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1284-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1284-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    CHENOPODIUM AMBROSIOIDES POLLEN 
    mexican tea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1285
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (CHENOPODIUM AMBROSIOIDES POLLEN - UNII:WIB701MW2H) CHENOPODIUM AMBROSIOIDES POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1285-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1285-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    CHENOPODIUM AMBROSIOIDES POLLEN 
    mexican tea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1286
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (CHENOPODIUM AMBROSIOIDES POLLEN - UNII:WIB701MW2H) CHENOPODIUM AMBROSIOIDES POLLEN0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1286-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1286-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    ZEA MAYS POLLEN 
    corn pollen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1121
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZEA MAYS POLLEN (UNII: 74PD8J616H) (ZEA MAYS POLLEN - UNII:74PD8J616H) ZEA MAYS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1121-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1121-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0626
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0626-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0626-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0627
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0627-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1600
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1600-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CAVIA PORCELLUS SKIN 
    guinea pig epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0653
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0653-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0653-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CAVIA PORCELLUS SKIN 
    guinea pig epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0654
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0654-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CAVIA PORCELLUS SKIN 
    guinea pig epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0655
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0655-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0655-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0628
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0628-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0628-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:0268-0628-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0629
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0629-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0629-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0865
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0865-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0865-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0866
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0866-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0867
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0867-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0868
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0868-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0868-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0869
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0869-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0870
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0870-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0870-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0871
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0871-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0871-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0878
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0878-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0878-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0879
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0879-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0879-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0880
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0880-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0880-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0881
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0881-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0882
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0882-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0882-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0886
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0886-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0886-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0887
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0887-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0888
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0888-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0889
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0889-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0890
    Route of AdministrationSUBCUTANEOUS
    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) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0890-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0891
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0891-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0892
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0892-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0892-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0893
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0893-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0894
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0894-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0894-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0895
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0895-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0895-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0896
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0896-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0897
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0897-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0898
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0898-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0899
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0899-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0899-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0900
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0900-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0901
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0901-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0901-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0902
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0902-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0902-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0903
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0903-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0904
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0904-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0905
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0905-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0906
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0906-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0911
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0911-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0911-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0912
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0912-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0912-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0913
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0913-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0913-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0914
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0914-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0914-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0915
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0915-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0916
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0916-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0916-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0917
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0917-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0917-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0918
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0918-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0919
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0919-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0920
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0920-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0921
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0921-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0921-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0922
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0922-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0922-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0923
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0923-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0923-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0924
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0924-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0925
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0925-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0926
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0926-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0926-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0928
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0928-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0928-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0929
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0929-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0929-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0930
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0930-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0930-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0932
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0932-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0932-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0933
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0933-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0931
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0931-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0934
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0934-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0934-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0935
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0935-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0935-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0936
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0936-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0936-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0937
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0937-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0937-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0939
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0939-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0939-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0957
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0957-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0957-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0958
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0958-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0959
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0959-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0959-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0961
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0961-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0961-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0962
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0962-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0963
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0963-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0965
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0965-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0966
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0966-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0967
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0967-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    SACCHAROMYCES CEREVISIAE 
    saccharomyces cerevisiae injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0968
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0968-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    SACCHAROMYCES CEREVISIAE 
    saccharomyces cerevisiae injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0969
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0969-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    ACACIA 
    acacia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1000
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O) ACACIA0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1000-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1000-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    ACACIA 
    acacia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1001
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O) ACACIA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1001-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1001-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    AILANTHUS ALTISSIMA POLLEN 
    ailanthus tree of heaven injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1004
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (AILANTHUS ALTISSIMA POLLEN - UNII:2A64U81OQ3) AILANTHUS ALTISSIMA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1004-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1004-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    ALNUS INCANA SSP RUGOSA POLLEN 
    alder white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1007
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1007-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1007-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    ALNUS INCANA SSP RUGOSA POLLEN 
    alder white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1008
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1008-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1008-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    ALNUS INCANA SSP RUGOSA POLLEN 
    alder white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1009
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1009-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MEDICAGO SATIVA POLLEN 
    alfalfa injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1012
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY) MEDICAGO SATIVA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1012-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1012-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MEDICAGO SATIVA POLLEN 
    alfalfa injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1013
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY) MEDICAGO SATIVA POLLEN1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1013-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS VELUTINA POLLEN 
    ash arizona injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1016
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD) FRAXINUS VELUTINA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1016-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS VELUTINA POLLEN 
    ash arizona injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1017
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD) FRAXINUS VELUTINA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1017-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS VELUTINA POLLEN 
    ash arizona injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1018
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD) FRAXINUS VELUTINA POLLEN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1018-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    FRAXINUS AMERICANA POLLEN 
    ash white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1021
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1021-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS AMERICANA POLLEN 
    ash white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1022
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1022-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1022-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS AMERICANA POLLEN 
    ash white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1023
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1023-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1023-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS AMERICANA POLLEN 
    ash white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1024
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1024-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1024-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS AMERICANA POLLEN 
    ash white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1025
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1025-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FRAXINUS AMERICANA POLLEN 
    ash white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1026
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1026-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    POPULUS TREMULOIDES POLLEN 
    aspen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1029
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (POPULUS TREMULOIDES POLLEN - UNII:928OC2TJDA) POPULUS TREMULOIDES POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1029-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1029-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    POPULUS TREMULOIDES POLLEN 
    aspen injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1030
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (POPULUS TREMULOIDES POLLEN - UNII:928OC2TJDA) POPULUS TREMULOIDES POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1030-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1030-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1033
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1033-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1034
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1034-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1034-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1035
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1035-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1035-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1036
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1036-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1036-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1037
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1037-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1038
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1038-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MORELLA CERIFERA POLLEN 
    bayberry wax myrtle injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1041
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1041-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1041-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MORELLA CERIFERA POLLEN 
    bayberry wax myrtle injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1042
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1042-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1042-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MORELLA CERIFERA POLLEN 
    bayberry wax myrtle injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1043
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1043-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FAGUS GRANDIFOLIA POLLEN 
    beech injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1046
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1046-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1046-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FAGUS GRANDIFOLIA POLLEN 
    beech injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1047
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1047-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1047-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FAGUS GRANDIFOLIA POLLEN 
    beech injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1048
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1048-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1048-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    FAGUS GRANDIFOLIA POLLEN 
    beech injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1049
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1049-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA LENTA POLLEN 
    birch black injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1056
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1056-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA LENTA POLLEN 
    birch black injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1057
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1057-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA LENTA POLLEN 
    birch black injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1058
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1058-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BETULA LENTA POLLEN 
    birch black injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1059
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN50000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1059-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA NIGRA POLLEN 
    birch river red injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1062
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1062-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA NIGRA POLLEN 
    birch river red injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1063
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1063-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1063-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA NIGRA POLLEN 
    birch river red injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1064
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1064-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BETULA NIGRA POLLEN 
    birch river red injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1065
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1065-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BETULA NIGRA POLLEN 
    birch river red injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1066
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1066-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1066-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BETULA LENTA POLLEN 
    birch white injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-1069
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-1069-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-1069-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0940
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0940-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0941
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0941-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0942
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0942-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0943
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0943-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0944
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0944-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    USTILAGO MAYDIS 
    corn smut injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0945
    Route of AdministrationSUBCUTANEOUS
    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
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0945-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0945-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    USTILAGO MAYDIS 
    corn smut injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0946
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0946-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    USTILAGO TRITICI 
    loose wheat smut injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0952
    Route of AdministrationSUBCUTANEOUS
    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) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0952-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0952-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0955
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0955-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0955-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0956
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0956-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0956-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0883
    Route of AdministrationSUBCUTANEOUS
    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
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0883-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0884
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0884-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0884-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:0268-0884-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0885
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0885-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0885-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0001
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0001-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0002
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0002-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0003
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0003-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0004
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0004-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0004-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0005
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0005-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0005-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0006
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0006-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0007
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0007-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0007-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0008
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST500 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0008-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0009
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0009-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0009-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0010
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0010-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0011
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0011-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0011-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0012
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0012-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0012-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    HOUSE DUST 
    house dust injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0013
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0013-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0013-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196506/30/2013
    BOS TAURUS SKIN 
    cattle epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0603
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0603-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0603-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BOS TAURUS SKIN 
    cattle epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0604
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0604-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BOS TAURUS SKIN 
    cattle epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0605
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0605-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BOS TAURUS SKIN 
    cattle epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0606
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0606-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    COTTON FIBER 
    cotton linters injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0609
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO) COTTON FIBER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0609-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0609-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    COTTON SEED 
    cottonseed injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0612
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COTTON SEED (UNII: DI0ZRJ0MXN) (COTTON SEED - UNII:DI0ZRJ0MXN) COTTON SEED0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0612-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0615
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0615-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0615-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0616
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0616-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0617
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0617-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0618
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0618-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0619
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0619-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0619-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0620
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0620-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0620-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0621
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.05 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0621-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0621-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0622
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0622-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0623
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.0005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0623-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0624
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0624-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0624-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0625
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0625-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0630
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0630-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0631
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0631-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0631-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0632
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0632-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0656
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0656-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0656-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    CEIBA PENTANDRA FIBER 
    kapok injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0635
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9) CEIBA PENTANDRA FIBER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0635-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0635-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUS MUSCULUS SKIN 
    mouse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0638
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0638-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0638-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    MUS MUSCULUS SKIN 
    mouse epithelia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0639
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0639-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    ORRIS 
    iris x germanica root injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0642
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IRIS X GERMANICA ROOT (UNII: 8N6VTJ9IWV) (IRIS X GERMANICA ROOT - UNII:8N6VTJ9IWV) IRIS X GERMANICA ROOT0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0642-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0642-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RABBIT 
    rabbit injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0649
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0649-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    RABBIT 
    rabbit injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0650
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0650-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    RABBIT 
    rabbit injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0651
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0651-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0651-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0705
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0705-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0706
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0706-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0706-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0707
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0707-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0707-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0708
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0708-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0709
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0709-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0710
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0710-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0711
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0711-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0714
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0714-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:0268-0714-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0715
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0715-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0716
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0716-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0717
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0268-0717-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10375301/01/196511/30/2021
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:0268-0718
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)