Label: Allergenic Extract

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    49288-0001-1, 49288-0001-2, 49288-0001-3, 49288-0001-4, view more
    49288-0001-5, 49288-0002-1, 49288-0002-2, 49288-0002-3, 49288-0002-4, 49288-0002-5, 49288-0003-1, 49288-0003-2, 49288-0003-3, 49288-0003-4, 49288-0003-5, 49288-0004-1, 49288-0004-2, 49288-0004-3, 49288-0004-4, 49288-0004-5, 49288-0005-1, 49288-0005-2, 49288-0005-3, 49288-0005-4, 49288-0005-5, 49288-0006-1, 49288-0006-2, 49288-0006-3, 49288-0006-4, 49288-0006-5, 49288-0007-1, 49288-0007-2, 49288-0007-3, 49288-0007-4, 49288-0007-5, 49288-0008-1, 49288-0008-2, 49288-0008-3, 49288-0008-4, 49288-0008-5, 49288-0030-1, 49288-0030-2, 49288-0030-3, 49288-0030-4, 49288-0030-5, 49288-0031-1, 49288-0031-2, 49288-0031-3, 49288-0031-4, 49288-0031-5, 49288-0032-1, 49288-0032-2, 49288-0032-3, 49288-0032-4, 49288-0032-5, 49288-0033-1, 49288-0033-2, 49288-0033-3, 49288-0033-4, 49288-0033-5, 49288-0035-1, 49288-0035-2, 49288-0035-3, 49288-0035-4, 49288-0035-5, 49288-0036-1, 49288-0036-2, 49288-0036-3, 49288-0036-4, 49288-0036-5, 49288-0037-1, 49288-0037-2, 49288-0037-3, 49288-0037-4, 49288-0037-5, 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49288-0651-4, 49288-0651-5
  • Packager: Antigen Laboratories, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated November 17, 2009

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • BOXED WARNING (What is this?)

    WARNINGS

    Allergenic extract is intended for use by, or under the guidance of, physicians who are experienced in the administration of allergenic extracts for diagnosis and/or immunotherapy and the emergency care of anaphylaxis. This extract is not directly interchangeable with other allergenic extracts. The initial dose must be based on skin testing as described in the “DOSAGE AND ADMINISTRATION” section of this insert. Patients switching from other types of extracts to Antigen Laboratories’ allergenic extracts should be started as if they were undergoing treatment for the first time. Patients being switched from one lot of extract to another from the same manufacturer should have the dose reduced by 75%.

    Severe systemic reactions may occur with all allergenic extracts. In certain individuals, especially in steroid-dependent/unstable asthmatics, these life-threatening reactions may result in death. Patients should be observed for at least 20 minutes following allergenic extract injections. Treatment and emergency measures, as well as personnel trained in their use, must be available in the event of a life-threatening reaction. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and/or death. Report serious adverse events to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787, phone 1-800-FDA-1088.

    This product should not be injected intravenously. Deep subcutaneous routes have proven to be safe. See the “WARNINGS”, “PRECAUTIONS”, “ADVERSE REACTIONS” and “OVERDOSAGE” sections.

    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 treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously. Refer to “WARNINGS”, “PRECAUTIONS” and “ADVERSE REACTIONS” sections below.

  • DESCRIPTION

    Antigen Laboratories’ allergenic extracts are manufactured from source material listed on the vial label. Lower concentrations (e.g. 1:50, 1:33, etc.) may be prepared either by dilution from a more concentrated stock or by direct extraction. The extract is a sterile solution containing extractables of source materials obtained from biological collecting and/or processing firms and Antigen Laboratories. All source materials are inspected by Antigen Laboratories’ technical personnel in accordance with 21 CFR 680.1 (b) (1). The route of administration for immunotherapy is subcutaneous. The routes of administration for diagnostic purposes are intradermal or prick-puncture of the skin.

    FOR ALLERGENIC EXTRACTS CONTAINING 50% V/V GLYCERINE AS PRESERVATIVE AND STABILIZER:

    INACTIVE INGREDIENTS:

    Sodium chloride…………………………………………………………….0.95%

    Sodium bicarbonate………………………………………………………..0.24%

    Glycerine…………………………………………………………………50% (v/v)

    Water for Injection…………………………………………………q.s. to volume

    Active allergens are described by common and scientific name on the stock concentrate container label or on last page of this circular.

    Food allergenic extracts may be manufactured on a weight/volume (w/v) or volume/volume (v/v) basis. Food extracts made from dried raw material are extracted at 2-10% (1:50-1:10 w/v ratio) in extracting fluid containing 50% glycerine. Slurries of juicy fruits or vegetables (prepared with a minimum amount of water for injection) are combined with an equal volume of glycerine for a ration of 1:1 volume/volume (v/v). Sodium chloride and sodium bicarbonate are added to the slurry and glycerine mixture. Fresh egg white extract is prepared by adding one part raw egg white to nine parts of extracting fluid (1:9 v/v).

    Antigen E is considered the most important allergen of Short Ragweed pollen and is used for the standardization of Short Ragweed allergenic extracts. Stock mixtures containing Short Ragweed are analyzed for Antigen E content by radial immunodiffusion using Center for Biologics Evaluation and Research (CBER) references and anti-serum. Antigen E content expressed as units of Antigen E per milliliter (U/ml) is printed on container label.

  • CLINICAL PHARMACOLOGY

    Studies indicate allergic individuals produce immunoglobulins of the IgE class in response to exposure to allergens. Subsequent exposure to the allergen results in a combination of allergen with IgE antibody fixed on mast cells or basophil membranes. This cross-linking results in stimulation of mast cell which leads to release and generation of pharmacologically active substances that produce immediate hypersensitivity reaction.3

    The mode of action of immunotherapy with allergenic extracts is still under investigation. Subcutaneous injections of increasing doses of allergenic extract into patients with allergic disease have been shown to result in both humoral and cellular changes including the production of allergen-specific IgG antibodies, the suppression of histamine release from target cells, decrease in circulating levels of antigen specific IgE antibody over long periods of time and suppression of peripheral blood T-lymphocyte cell responses to antigen.10, 14, 15

  • INDICATIONS AND USAGE

    Allergenic extract is used for diagnostic testing and for the treatment (immunotherapy) of patients whose histories indicate that upon natural exposure to the allergen, they experience allergic symptoms. Confirmation is determined by skin testing. Diagnostic use of allergenic extracts usually begins with direct skin testing. This product is not intended for treatment of patients who do not manifest immediate hypersensitivity reactions to the allergenic extract following skin testing.

  • CONTRAINDICATIONS

    Do not administer in the presence of diseases characterized by bleeding diathesis. Individuals with autoimmune disease may be at risk of exacerbating symptoms of the underlying disease, possibly due to routine immunization. Patients who have experienced a recent myocardial infarction may not be tolerant of immunotherapy. Children with nephrotic syndrome probably should not receive injections due to immunization causing exacerbation of nephrotic disease.

  • WARNINGS

    Refer to boxed “WARNINGS”, “PRECAUTIONS”, “ADVERSE REACTIONS” and “OVERDOSAGE” sections for additional information on serious adverse reactions and steps to be taken, if any occur.

    Extreme caution is necessary when using diagnostic skin tests or injection treatment in highly sensitive patients who have experienced severe symptoms or anaphylaxis by natural exposure, or during previous skin testing or treatment. IN THESE CASES THE POTENCY FOR SKIN TESTS AND THE ESCALATION OF THE TREATMENT DOSE MUST BE ADJUSTED TO THE PATIENT’S SENSITIVITY AND TOLERANCE.

    Benefit versus risk needs to be evaluated in steroid dependent asthmatics, patients with unstable asthma or patients with underlying cardiovascular disease.

    Injections should never be given intravenously. A 5/8 inch, 25 gauge needle on a sterile syringe allows deep subcutaneous injection. Withdraw plunger slightly after inserting needle to determine if a blood vessel has been entered.

    Proper measurement of dose and caution in making injection will minimize reactions. Adverse reactions to allergenic extracts are usually apparent within 20-30 minutes following injection of immunotherapy.

    Extract should be temporarily withheld or dosage reduced in case of any of the following conditions: 1) flu or other infection with fever; 2) exposure to excessive amounts of allergen prior to injection; 3) rhinitis and/or asthma exhibiting severe symptoms; 4) adverse reaction to previous injection until cause of reaction has been evaluated by physician supervising patient’s immunotherapy program.

  • PRECAUTIONS

    General:

    Immunotherapy must be given under physician’s supervision. Sterile solutions, vials, syringes, etc. must be used. Aseptic technique must be observed in making dilutions from stock concentrates. The usual precautions in administering allergenic extracts are necessary, refer to boxed WARNINGS and “WARNINGS” section. Sterile syringe and needle must be used for each individual patient to prevent transmission of serum hepatitis, Human Immunodeficiency Virus (HIV) and other infectious agents.

    Epinephrine 1:1000 should be available. Refer to “OVERDOSAGE” section for description of treatment for anaphylactic reactions.

    Information for Patients:

    Patient should remain under observation of a nurse, physician, or personnel trained in emergency measures for at least 20 minutes following immunotherapy injection. Patient must be instructed to report any adverse reactions that occur within 24 hours after injection. Possible adverse reactions include unusual swelling and/or tenderness at injection site, rhinorrhea, sneezing, coughing, wheezing, shortness of breath, nausea, dizziness, or faintness. Immediate medical attention must be sought for reactions that occur during or after leaving physician’s office.

    Carcinogenesis, Mutagenesis, Impairment of Fertility:

    Long term studies in animals have not been conducted with allergenic extract to determine their potential for carcinogenicity, mutagenicity or impairment of fertility.

    Pregnancy Category C:

    Animal reproduction studies have not been conducted with allergenic extracts. It is not known whether allergenic extracts cause fetal harm during pregnancy or affect reproductive capacity. A systemic reaction to allergenic extract could cause uterine contractions leading to spontaneous abortion or premature labor. Allergenic extracts should be used during pregnancy only if potential benefit justifies potential risk to fetus.11

    Nursing Mothers:

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

    Pediatric Use:

    Allergenic extracts have been used routinely in children, and no special safety problems or specific hazards have been found. Children can receive the same dose as adults. Discomfort is minimized by dividing the dose in half and administering injection at two different sites.16, 17

    Drug Interactions:

    Antihistamines. Antihistamines inhibit the wheal and flare reaction. The inhibitory effect of conventional antihistamines varies from 1 day up to 10 days, according to the drug and patient’s sensitivity. Long acting antihistamines (e.g., astemizole) may inhibit the wheal and flare for up to forty days.1, 2

    Imipramines, phenothiazines, and tranquilizers. Tricyclic antidepressants exert a potent and sustained decrease of skin reactions to histamine. This effect may last for a few weeks. Tranquilizers and antiemetic agents of the phenothiazine class have H1 antihistaminic activity and can block skin tests.1

    Corticosteroids. Short-term (less than 1 week) administration of corticosteroids at the therapeutic doses used in asthmatic patients does not modify the cutaneous reactivity to histamine, compound 48/80, or allergen. Long-term corticosteroid therapy modifies the skin texture and makes the interpretation of immediate skin tests more difficult.1

    Theophylline. It appears that theophylline need not be stopped prior to skin testing.1

    Beta-Blockers. Patients receiving beta-blockers may not be responsive to epinephrine or inhaled bronchodilators. The following are commonly prescribed beta-blockers: Levatol, Lopressor, Propanolol Intersol, Propanolol HCL, Blocadren, Propanolol, Inderal-LA, Visken, Corgard, Ipran, Tenormin, Timoptic. Ophthalmic beta-blockers: Betaxolol, Levobunolol, Timolol, Timoptic. Chemicals that are beta-blockers and may be components of other drugs: Acebutolol, Atenolol, Esmolol, Metoprolol, Nadolol, Penbutolol, Pindolol, Propanolol, Timolol, Labetalol, Carteolol.1

    Beta-adrenergic agents. Inhaled beta2 agonists in the usual doses used for the treatment of asthma do not usually inhibit allergen-induced skin tests. However, oral terbutaline and parenteral ephedrine were shown to decrease the allergen-induced wheal.1

    Cromolyn. Cromolyn inhaled or injected prior to skin tests with allergens or degranulating agents does not alter skin whealing response.1

    Other drugs. Other drugs have been shown to decrease skin test reactivity. Among them, dopamine is the best-documented compound.1

    Specific Immunotherapy. A decreased skin test reactivity has been observed in patients undergoing specific immunotherapy with pollen extracts, grass pollen allergoids, mites, hymenoptera venoms, or in professional beekeepers who are spontaneously desensitized. Finally, it was shown that specific immunotherapy in patients treated with ragweed pollen extract induced a decreased late-phase reaction.1

  • ADVERSE REACTIONS

    Adverse reactions include, but are not limited to urticaria; itching; edema of extremities; respiratory wheezing or asthma; dyspnea; cyanosis; tachycardia; lacrimation; marked perspiration; flushing of face, neck or upper chest; mild persistent clearing of throat; hacking cough or persistent sneezing.

    1) Local Reactions

    A mild burning immediately after injection is expected; this usually subsides in 10-20 seconds. Prolonged pain or pain radiating up arm is usually the result of intramuscular injection, making this injection route undesirable. Subcutaneous injection is the recommended route.

    Small amounts of erythema and swelling at the site of injection are common. Reactions should not be considered significant unless they persist for at least 24 hours or exceed 50 mm in diameter.

    Larger local reactions are not only uncomfortable, but indicate the possibility of a severe systemic reaction if dosage is increased. In such cases dosage should be reduced to the last level not causing reaction and maintained for two or three treatments before cautiously increasing.

    Large, persistent local reactions or minor exacerbations of the patient’s allergic symptoms may be treated by local cold applications and/or use of oral antihistamines.

    2) Systemic Reactions

    Systemic reactions range from mild exaggeration of patient’s allergic symptoms to anaphylactic reactions.14 Very sensitive patients may show a rapid response. It cannot be overemphasized that, under certain unpredictable combinations of circumstances, anaphylactic shock is always a possibility. Fatalities are rare but can occur.5 Other possible systemic reaction symptoms are fainting, pallor, bradycardia, hypotension, angioedema, cough, wheezing, conjunctivitis, rhinitis,and urticaria.13, 14

    Careful attention to dosage and administration limit such reactions. 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 prepare for treatment of severe reactions. Refer to “OVERDOSAGE” section.

  • OVERDOSAGE

    Refer to “WARNINGS”, “PRECAUTIONS” and “ADVERSE REACTIONS” sections for signs and symptoms of an overdose.

    If a systemic or anaphylactic reaction does occur, apply tourniquet above the site of allergenic extract injection and inject intramuscularly or subcutaneously 0.3 to 0.5 ml of 1:1000 Epinephrine-hydrochloride into the opposite arm or gluteal area. Repeat dose in 5-10 minutes if necessary. Loosen tourniquet briefly at 5 minute intervals to prevent circulatory impairment. Discontinue use of the tourniquet after ½ hour.

    The epinephrine HCL 1:1000 dose for infants to 2 years is 0.05 to 0.1 ml; for children 2 to 6 years it is 0.15 ml; for children 6 to 12 years it is 0.2 ml.

    Symptoms of progressive anaphylaxis include airway obstruction and/or vascular collapse. After administration of epinephrine, profound shock and vasomotor collapse should be treated with intravenous fluids and possibly vasoactive drugs. Monitor airways for obstruction. Oxygen should be given by mask if indicated.

    Antihistamines, H2 antagonist, bronchodilators, steroids and theophylline may be used as indicated after providing adequate epinephrine and circulatory support.4

    Patients who have been taking beta-blockers may be unresponsive to epinephrine. Epinephrine or beta-adrenergic drugs (Alupent) may be ineffective. These drugs should be administered even though a beta-blocker may have been taken. The following treatment will be effective whether or not patient is taking a beta-blocker: Aminophylline IV, slow push or drip, Atrovent (Ipratropium bromide) Inhaler, 3 inhalations repeated, Atropine, 0.4 mg/ml, 0.75 to 1.5 ml IM or IV, Solu-Cortef, 100-200 mg IM or IV, Solu-Medrol, 125 mg IM or IV, Glucagon, 0.5-1 mg IM or IV, Benadryl, 50 mg IM or IV, Cimetidine, 300 mg IM or IV, Oxygen via ambu bag.

  • DOSAGE AND ADMINISTRATION

    Refer to “STORAGE” section for proper storage condition for allergenic extract. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Some allergenic extracts naturally precipitate.

    Physicians undertaking immunotherapy should be concerned with patient’s degree of sensitivity. The initial dilution of allergenic extract, starting dose, and progression of dosage must be carefully determined on the basis of the patient’s history and results of skin tests. Strongly positive skin tests may be risk factors for systemic reactions. Less aggressive immunotherapy schedules may be indicated for such patients.

    Precaution is necessary when using extract mixture for skin testing. The diluting effect of individual components within a mixture may cause false negative reactions. Patients extremely sensitive to a common allergen in several components of a mixture may be more likely to experience a systemic reaction than when skin tested individually for each component.9

    PRICK-PUNCTURE TESTING: To identify highly sensitive individuals and as a safety precaution, it is recommended that a prick-puncture test using a drop of the extract concentrate be performed prior to initiating very dilute intradermal testing. Prick-puncture testing is performed by placing a drop of extract concentrate on the skin and puncturing the skin through the drop with a small needle such as a bifurcated vaccinating needle. The most satisfactory sites on the back for skin testing are from the posterior axillary fold to 2.5 cm from the spinal column, and from the top of the scapula to the lower rib margins. The best areas on the arms are the volar surfaces from the axilla to 2.5 or 5 cm above the wrist, skipping the anticubital space. A positive reaction is approximately 10-15 mm erythema with 2.5 mm wheal. Smaller, less conclusive reactions may be considered positive in conjunction with a definitive history of symptoms on exposure to the allergen. The more sensitive the patient the higher the probability that he/she will have symptoms related to the exposure of the offending allergen. Hence, the importance of a good patient history. Less sensitive individuals can be tested intradermally with an appropriately diluted extract.

    A positive control using histamine phosphate identifies patients whose skin may not react due to medications, metabolic or other reasons. A negative control (50% glycerine for prick-puncture testing) would exclude false-positive reactions due to ingredients in diluent or patients who have dermatographism.

    SINGLE DILUTION INTRADERMAL TESTING: The surface of the upper and lower arm is the usual location for skin testing. It is important that a new, sterile, disposable syringe and needle be used for each extract tested. Intracutaneous test dilutions, five-fold or ten-fold, may be prepared from stock concentrate using physiologic saline as a diluent. (1) Start testing with the most dilute allergenic extract concentration. (2) A volume of 0.02-0.05 ml should be injected slowly into the superficial skin layers making a small bleb (superficial wheal). (3) For patients without a history of extreme sensitivity, or a negative or weakly reactive prick-puncture test, the initial dilution for skin testing should be a dilution at least 1:12,500 w/v. This initial dilution can be prepared by diluting 1:20 to 1:50 w/v (2%-5%) extracts five-fold to 5-4 or 1:10 w/v (10%) extracts to 5-5. See “Serial Dilutions Titration Test Dilutions” chart on the next page. Dilute 1:10 w/v (10%) extracts to 10-3 if using ten-fold dilutions. (4) Sensitive patients with a positive prick-puncture test require a further dilution to at least 1:312,500 w/v. This dilution can be prepared by diluting 1:20 to 1:50 w/v (2% - 5%) extracts to 5-6 or 1:10 w/v (10%) extracts to 5-7 (five-fold dilutions). Ten-fold dilution to 10-6 of a 1:10 w/v (10%) extract would be a safe starting dilution. Size of reactions are quantitated based on size of wheal and erythema. For interpretation of skin reactions, refer to chart below. If after 20 minutes no skin reaction is observed, continue testing using increasing increments of the concentration until a reaction of 5-10 mm wheal and 11-30 mm erythema is obtained, or a concentration of 5-2 or 10-1 has been tested. A negative control, 50% glycerine diluted with diluent to 5-2 (1:25) or 10-1 (1:10) dilution and a positive control of histamine phosphate, should be tested and included in interpretation of skin reactions.1, 13

    GRADEmm ERYTHEMAmm WHEAL
    0less than 5less than 5
    ±5-105-10
    1+11-205-10
    2+21-305-10
    3+31-4010-15 or with pseudopods
    4+greater than 40greater than 15 or with many pseudopods

    INTRADERMAL TESTING-SKIN ENDPOINT TITRATION: The allergenic extracts to which the patient is sensitive, the patient’s degree of sensitivity and the dose of allergen to be used in immunotherapy can be determined through the use of intracutaneous skin tests involving progressive five-fold dilutions of allergenic extracts. Intracutaneously inject 0.01 to 0.02 ml of the test allergen to form a 4 mm diameter superficial skin wheal. For patients demonstrating a negative or weakly reactive prick-puncture skin test, an initial screening dilution of 1:12,500 w/v is safe. For patients demonstrating a positive prick-puncture skin test, an initial screening dilution of 1:312,500 w/v is safe. (See “Serial Dilution Titration Test Dilutions” chart below.) When a sequence of five-fold or ten-fold dilutions of an allergen are injected, the endpoint is determined by noting the dilution that first produces a wheal and erythema (15 minutes after injection) that is 2 mm larger than wheals with erythema produced by weaker, non-reacting dilutions (5 mm negative wheal). The endpoint dilution is used as a starting dose concentration for immunotherapy. An endpoint dose of 0.15 ml is a safe initial dose to be followed by escalation to the optimal maximum tolerated dose for each individual.

    Injections should never be given intravenously. A 5/8 inch, 25 gauge needle on a sterile syringe will allow deep subcutaneous injection.

    IMMUNOTHERAPY: If the first injection of the initial dilution of extract is tolerated without significant local reaction, increasing doses by 5-20% increments of that dilution may be administered. The rate of increase in dosage in the early stages of treatment with highly diluted extracts is usually more rapid than the rate of increase possible with more concentrated extracts. This schedule is intended only as a guide and must be modified according to the reactivity of the individual patient. Needless to say, the physician must proceed cautiously in the treatment of the highly sensitive patient who develops large local or systemic reactions.6

    Some patients may tolerate larger doses of the allergenic extract depending on patient response.7 Because diluted extract tends to lose activity in storage, the first dose from a more concentrated vial should be the same, or less than, the previous dose.8, 12

    Dosages progressively increase according to the tolerance of the patient at intervals of one to seven days until, (1) the patient achieves relief from symptoms, (2) induration at the site of injection is no larger than 50 mm in 36 to 48 hours, (3) a maintenance dose is reached (the largest dose tolerated by the patient that relieves symptoms without undesirable local or systemic reactions). This maintenance dose may be continued at regular intervals perennially. It may be necessary to adjust the progression of dosage downward to avoid local and constitutional reactions.

    The usual duration of treatment has not been established. A period of two or three years on immunotherapy constitutes an average minimum course of treatment.

    SERIAL DILUTION TITRATION TEST DILUTIONS APPROXIMATE ALLERGENIC EXTRACT CONCENTRATION RESULTING FROM 1:5 DILUTION
    Titration NumberDilution ExponentWeight / VolumeAllergenic Extract Concentrate
    1:50 (2%)1:40 (2 1/2%)1:33 1/3 (3%)1:20 (5%)1:10 (10%)
    No. 15-11:51:2501:2001:1671:1001:50
    No. 25-21:251:1,2501:1,0001:8351:5001:250
    No. 35-31:1251:6,2501:5,0001:4,1751:2,5001:1,250
    No. 45-41:6251:31,2501:25,0001:20,8751:12,5001:6,250
    No. 55-51:3,1251:156,2501:125,0001:104,3751:62,5001:31,250
    No. 65-61:15,6251:781,2501:625,0001:521,8751:312,5001:156,250
    No. 75-71:78,1251:3,906,2501:3,125,0001:2,609,3751:1,562,5001:781,250
    No. 85-81:390,6251:19,531,2501:15,625,0001:13,046,8751:7,812,5001:3,906,250
    No. 95-91:1,953,1251:97,656,2501:78,125,0001:65,234,3751:39,062,5001:19,531,250
    No. 105-101:9,765,6251:488,281,2501:390,625,0001:326,171,8751:195,312,5001:97,656,250
    No. 115-111:48,828,1251:2,441,406,2501:1,953,125,0001:1,630,859,3751:976,562,5001:488,281,250
    No. 125-121:244,140,6251:12,207,031,2501:9,765,625,0001:8,154,296,8751:4,882,812,5001:2,441,406,250
  • HOW SUPPLIED

    Stock concentrates are available in concentrations of 2-10% or weight/volume (w/v) of 1:50, 1:33, 1:20 or 1:10. Some juicy or liquid foods are available at 1:1 volume/volume (v/v) extraction ratio. Fresh egg white extract is available at 1:9 v/v extraction ratio.

    Antigen E content of ragweed mixtures ranges from 46-166 U/ml for Ragweed Mixture (Short/Giant/Western/Southern Ragweed), 47-239 U/ml for Short/Giant/Western Ragweed Mixture, and 106-256 U/ml for Short/Giant Ragweed Mixture. Refer to container label for actual Antigen E content.

    Extract (stock concentrate) is supplied in 10, 30 and 50 ml containers. Extracts in 5 ml dropper bottles are available for prick-puncture testing. To insure maximum potency for the entire dating period, all stock concentrates contain 50% glycerine v/v.

  • STORAGE

    Store all stock concentrates and dilutions at 2-8° C. Keep at this temperature during office use. The expiration date of the allergenic extracts is listed on the container label. Dilutions of the allergenic extracts containing less than 50% glycerine are less stable. If loss of potency is suspected, potency can be checked using side by side skin testing with freshly prepared dilutions of equal concentration on individuals with known sensitivity to the allergen.

  • REFERENCES

    1. Bousquet, Jean: “In vivo methods for study of allergy: Skin tests” Third Edition, Allergy Principles and Practice, C.V. Mosby Co., Vol. I, Chap. 19, pp 419-436, 1988.

    2. Long, W.F., Taylor, R.J., Wagner, C.J., et al.: Skin test suppression by antihistamines and the development of subsensitivity, J. Allergy Clin. Immunol., pp. 76-113, 1985.

    3. Holgate, S.T., Robinson, C., Church, Mike: Mediators of Immediate Hypersensitivity, Third Edition, Allergy Principles and Practice, C.V. Mosby Co., Vol. I and II, pp 135-163, 1988.

    4. Wasserman, S., Marquart, D.: Anaphylaxis, Third Edition, Allergy Principles and Practice, C.V. Mosby Co., Vol. 1, Chap. 58, pp. 1365-1376, 1988.

    5. Reid, Michael J., Lockey, Richard F., Turkeltaub M.D., Paul C., Platts-Mills, Thomas. “Survey of Fatalities from Skin Testing and Immunotherapy 1985-1989”, Journal of Allergy and Clinical Immunology, Vol. 92, No. 1, pp. 6-15, 1993.

    6. Matthews, K., et al: Rhinitis, Asthma and Other Allergic Diseases. NIAID Task Force Report, U.S. Dept. HEW, NIH Publication No. 79-387, Chapter 4, pp. 213-217, May 1979.

    7. Ishizaka, K.: Control of IgE Synthesis, Third Edition, Allergy Principles and Practices, Vol. I, Chap. 4, p. 52, edited by Middleton et al.

    8. Nelson, H.S.: “The Effect of Preservatives and Dilution on the Deterioration of Russian Thistle (Salsola pestifer), a pollen extract.” The Journal of Allergy and Clinical Immunology, Vol. 63, No. 6, pp. 417-425, June 1979.

    9. Seebohm, P.M., et al: Panel on Review of Allergenic Extracts, Final Report, Food and Drug Administration, March 13, 1981, pp. 84-86.

    10. Rocklin, R.E., Sheffer, A.L., Grainader, D.K. and Melmon, K.: “Generation of antigen-specific suppressor cells during allergy desensitization”, New England Journal of Medicine, 302, May 29, 1980, pp. 1213-1219.

    11. Seebohm, P.M., et al: Panel on Review of Allergenic Extracts, Final Report, Food and Drug Administration, March 13, 1981, pp 9-48.

    12. Stevens, E.: Cutaneous Tests, Regulatory Control and Standardization of Allergenic Extracts, First International Paul-Ehrlich Seminar, May 20-22, 1979, Frankfurt, Germany, pp. 133-138.

    13. Van Metre, T., Adkinson, N., Amodio, F., Lichtenstein, L., Mardinay, M., Norman, P., Rosenberg, G., Sobotka, A., Valentine, M.: “A Comparative Study of the Effectiveness of the Rinkel Method and the Current Standard Method of Immunology for Ragweed Pollen Hay Fever,“ The Journal of Clinical Allergy and Immunology, Vol. 66, No. 6, p. 511, December 1980.

    14. Wasserman, S.: The Mast Cell and the Inflammatory Response. The Mast Cell-its role in Health and disease. Edited by J. Pepys & A.M. Edwards, Proceedings of an International Symposium, Davos, Switzerland, Pitman Medical Publishing Co., 1979, pp. 9-20.

    15. Perelmutter, L.: IgE Regulation During Immunotherapy of Allergic Diseases. Annals of Allergy, Vol. 57, August 1986.

    16. Bullock, J., Frick, O.: Mite Sensitivity in House Dust Allergic Children, Am. J. Dis. Child., pp. 123-222, 1972.

    17. Willoughby, J.W.: Inhalant Allergy Immunotherapy with Standardized and Nonstandardized Allergenic Extracts, American Academy of Otolaryngology-Head and Neck Surgery: Instructional Courses, Vol. 1, Chapter 15, C.V. Mosby Co., St. Louis, Missouri, September 1988.

  • CONTAINER LABELING

    5 mL Green Label
    10 mL Green Label
    30/50 mL Green Label
  • INGREDIENTS AND APPEARANCE
    CHAETOMIUM 
    chaetomium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0094
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0094-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0094-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0094-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0094-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0094-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CEPHALOSPORIUM 
    cephalosporium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0089
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0089-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0089-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0089-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0089-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0089-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CLADOSPORIUM HERBARUM 
    cladosporium herbarum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0159
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0159-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0159-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0159-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0159-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0159-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CURVULARIA 
    curvularia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0098
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0098-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0098-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0098-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0098-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0098-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    BOTRYTIS 
    botrytis injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0039
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0039-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0039-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0039-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0039-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0039-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ASPERGILLUS NIGER 
    aspergillus niger injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0033
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0033-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0033-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0033-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0033-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0033-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/23/1974
    CEPHALOSPORIUM 
    cephalosporium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0088
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0088-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0088-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0088-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0088-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0088-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    BERMUDA GRASS SMUT 
    bermuda grass smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0065
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0065-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0065-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0065-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0065-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0065-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    HELMINTHOSPORIUM 
    helminthosporium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0249
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0249-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0249-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0249-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0249-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0249-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    HELMINTHOSPORIUM 
    helminthosporium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0248
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0248-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0248-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0248-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0248-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0248-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    JOHNSON GRASS SMUT 
    johnson grass smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0280
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0280-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0280-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0280-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0280-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0280-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    JOHNSON GRASS SMUT 
    johnson grass smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0279
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0279-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0279-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0279-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0279-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0279-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    FUSARIUM OXYSPORUM 
    fusarium oxysporum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0198
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0198-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0198-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0198-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0198-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0198-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    EPICOCCUM 
    epicoccum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0187
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0187-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0187-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0187-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0187-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0187-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    HORMODENDRUM 
    hormodendrum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0246
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0246-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0246-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0246-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0246-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0246-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    HORMODENDRUM 
    hormodendrum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0245
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0245-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0245-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0245-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0245-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0245-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NUMBER FOUR MOLD MIXTURE 
    number four mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0210
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.0125 g  in 1 mL
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0031 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0031 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0031 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0031 g  in 1 mL
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.0125 g  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0021 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0021 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0021 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0021 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0021 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0021 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0210-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0210-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0210-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0210-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0210-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    GRASS SMUT MIXTURE 
    grass smut mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0214
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.05 g  in 1 mL
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0214-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0214-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0214-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0214-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0214-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    GRAIN SMUT MIXTURE 
    grain smut mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0211
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO NUDA HORDEI (UNII: 9Y53ZS6I82) (USTILAGO NUDA HORDEI - UNII:9Y53ZS6I82) USTILAGO NUDA HORDEI0.025 g  in 1 mL
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.025 g  in 1 mL
    USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.025 g  in 1 mL
    USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0211-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0211-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0211-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0211-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0211-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    A MOLD MIXTURE 
    a mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0004
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0017 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0017 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0017 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0017 g  in 1 mL
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.0067 g  in 1 mL
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.0067 g  in 1 mL
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.0067 g  in 1 mL
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.0067 g  in 1 mL
    GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.0067 g  in 1 mL
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0067 g  in 1 mL
    CANDIDA TROPICALIS (UNII: Q222J2186W) (CANDIDA TROPICALIS - UNII:Q222J2186W) CANDIDA TROPICALIS0.0033 g  in 1 mL
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.0033 g  in 1 mL
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0022 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.0022 g  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0011 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0011 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0011 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0011 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0011 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0011 g  in 1 mL
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.0067 g  in 1 mL
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0067 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0067 g  in 1 mL
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA0.0067 g  in 1 mL
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.0067 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0022 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0004-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0004-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0004-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0004-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0004-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    MICROSPORUM CANIS 
    microsporum canis injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0299
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICROSPORUM CANIS (UNII: N4F4RQ7BY7) (MICROSPORUM CANIS - UNII:N4F4RQ7BY7) MICROSPORUM CANIS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0299-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0299-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0299-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0299-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0299-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    B MOLD MIXTURE 
    b mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0035
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.0071 g  in 1 mL
    PASSALORA FULVA (UNII: HR6H5057CO) (PASSALORA FULVA - UNII:HR6H5057CO) PASSALORA FULVA0.0071 g  in 1 mL
    COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.0071 g  in 1 mL
    MYROTHECIUM VERRUCARIA (UNII: W5U19AK212) (MYROTHECIUM VERRUCARIA - UNII:W5U19AK212) MYROTHECIUM VERRUCARIA0.0071 g  in 1 mL
    HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U) HYPOMYCES PERNICIOSUS0.0071 g  in 1 mL
    NEUROSPORA CRASSA (UNII: 1X92VM01YP) (NEUROSPORA CRASSA - UNII:1X92VM01YP) NEUROSPORA CRASSA0.0071 g  in 1 mL
    KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE0.0071 g  in 1 mL
    PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.0071 g  in 1 mL
    MICROASCUS BREVICAULIS (UNII: DHI513VXU7) (MICROASCUS BREVICAULIS - UNII:DHI513VXU7) MICROASCUS BREVICAULIS0.0071 g  in 1 mL
    COLLETOTRICHUM COCCODES (UNII: Y0M7LGE3Z8) (COLLETOTRICHUM COCCODES - UNII:Y0M7LGE3Z8) COLLETOTRICHUM COCCODES0.0071 g  in 1 mL
    PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (PLEOSPORA HERBARUM - UNII:0N3Z1P4B2W) PLEOSPORA HERBARUM0.0071 g  in 1 mL
    STREPTOMYCES GRISEUS (UNII: G0O5980Z7W) (STREPTOMYCES GRISEUS - UNII:G0O5980Z7W) STREPTOMYCES GRISEUS0.0071 g  in 1 mL
    TRICHODERMA VIRIDE (UNII: T8678F0P0Q) (TRICHODERMA VIRIDE - UNII:T8678F0P0Q) TRICHODERMA VIRIDE0.0071 g  in 1 mL
    TRICHOPHYTON SCHOENLEINII (UNII: Z4MD1809H1) (TRICHOPHYTON SCHOENLEINII - UNII:Z4MD1809H1) TRICHOPHYTON SCHOENLEINII0.0071 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0035-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0035-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0035-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0035-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0035-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    ASPERGILLUS MIXTURE 
    aspergillus mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0007
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0025 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0025 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0025 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0007-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0007-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0007-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0007-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0007-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ALTERNARIA ALTERNATA 
    alternaria alternata injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0002
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0002-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0002-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0002-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0002-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0002-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NUMBER TEN MOLD MIXTURE 
    number ten mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0586
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.01 g  in 1 mL
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0025 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0025 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0025 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0025 g  in 1 mL
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.01 g  in 1 mL
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.01 g  in 1 mL
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.01 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.01 g  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0017 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0017 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0017 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0017 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0017 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0017 g  in 1 mL
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.01 g  in 1 mL
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.01 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0586-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0586-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0586-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0586-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0586-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0031
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0031-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0031-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0031-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0031-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0031-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ALTERNARIA ALTERNATA 
    alternaria alternata injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0003
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0003-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0003-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0003-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0003-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0003-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MUCOR MIXTURE 
    mucor mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0294
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0333 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.0333 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0333 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0294-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0294-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0294-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0294-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0294-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    MONILIA MIXTURE 
    monilia mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0293
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA TROPICALIS (UNII: Q222J2186W) (CANDIDA TROPICALIS - UNII:Q222J2186W) CANDIDA TROPICALIS0.025 g  in 1 mL
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0293-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0293-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0293-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0293-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0293-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON MIXTURE 
    trichophyton mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0576
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.05 g  in 1 mL
    TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0576-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0576-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0576-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0576-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0576-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    PENICILLIUM MIXTURE 
    penicillium mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0363
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0167 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0167 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0167 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0167 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0167 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0167 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0363-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0363-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0363-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0363-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0363-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    GRAIN SMUT MIXTURE 
    grain smut mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0213
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO NUDA HORDEI (UNII: 9Y53ZS6I82) (USTILAGO NUDA HORDEI - UNII:9Y53ZS6I82) USTILAGO NUDA HORDEI0.005 g  in 1 mL
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.005 g  in 1 mL
    USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.005 g  in 1 mL
    USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0213-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0213-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0213-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0213-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0213-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222309/09/1997
    GRAIN SMUT MIXTURE 
    grain smut mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0212
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO NUDA HORDEI (UNII: 9Y53ZS6I82) (USTILAGO NUDA HORDEI - UNII:9Y53ZS6I82) USTILAGO NUDA HORDEI0.0125 g  in 1 mL
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.0125 g  in 1 mL
    USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.0125 g  in 1 mL
    USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI0.0125 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0212-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0212-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0212-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0212-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0212-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222309/09/1997
    GRASS SMUT MIXTURE 
    grass smut mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0216
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.01 g  in 1 mL
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0216-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0216-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0216-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0216-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0216-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    GRASS SMUT MIXTURE 
    grass smut mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0215
    Route of AdministrationSUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.025 g  in 1 mL
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0215-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0215-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0215-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0215-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0215-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    B MOLD MIXTURE 
    b mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0037
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.0018 g  in 1 mL
    PASSALORA FULVA (UNII: HR6H5057CO) (PASSALORA FULVA - UNII:HR6H5057CO) PASSALORA FULVA0.0018 g  in 1 mL
    COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.0018 g  in 1 mL
    MYROTHECIUM VERRUCARIA (UNII: W5U19AK212) (MYROTHECIUM VERRUCARIA - UNII:W5U19AK212) MYROTHECIUM VERRUCARIA0.0018 g  in 1 mL
    HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U) HYPOMYCES PERNICIOSUS0.0018 g  in 1 mL
    NEUROSPORA CRASSA (UNII: 1X92VM01YP) (NEUROSPORA CRASSA - UNII:1X92VM01YP) NEUROSPORA CRASSA0.0018 g  in 1 mL
    KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE0.0018 g  in 1 mL
    PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.0036 g  in 1 mL
    MICROASCUS BREVICAULIS (UNII: DHI513VXU7) (MICROASCUS BREVICAULIS - UNII:DHI513VXU7) MICROASCUS BREVICAULIS0.0018 g  in 1 mL
    COLLETOTRICHUM COCCODES (UNII: Y0M7LGE3Z8) (COLLETOTRICHUM COCCODES - UNII:Y0M7LGE3Z8) COLLETOTRICHUM COCCODES0.0018 g  in 1 mL
    PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (PLEOSPORA HERBARUM - UNII:0N3Z1P4B2W) PLEOSPORA HERBARUM0.0018 g  in 1 mL
    STREPTOMYCES GRISEUS (UNII: G0O5980Z7W) (STREPTOMYCES GRISEUS - UNII:G0O5980Z7W) STREPTOMYCES GRISEUS0.0018 g  in 1 mL
    TRICHODERMA VIRIDE (UNII: T8678F0P0Q) (TRICHODERMA VIRIDE - UNII:T8678F0P0Q) TRICHODERMA VIRIDE0.0018 g  in 1 mL
    TRICHOPHYTON SCHOENLEINII (UNII: Z4MD1809H1) (TRICHOPHYTON SCHOENLEINII - UNII:Z4MD1809H1) TRICHOPHYTON SCHOENLEINII0.0018 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0037-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0037-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0037-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0037-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0037-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    B MOLD MIXTURE 
    b mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0036
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.0036 g  in 1 mL
    PASSALORA FULVA (UNII: HR6H5057CO) (PASSALORA FULVA - UNII:HR6H5057CO) PASSALORA FULVA0.0036 g  in 1 mL
    COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.0036 g  in 1 mL
    MYROTHECIUM VERRUCARIA (UNII: W5U19AK212) (MYROTHECIUM VERRUCARIA - UNII:W5U19AK212) MYROTHECIUM VERRUCARIA0.0036 g  in 1 mL
    HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U) HYPOMYCES PERNICIOSUS0.0036 g  in 1 mL
    NEUROSPORA CRASSA (UNII: 1X92VM01YP) (NEUROSPORA CRASSA - UNII:1X92VM01YP) NEUROSPORA CRASSA0.0036 g  in 1 mL
    KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE0.0036 g  in 1 mL
    PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.0036 g  in 1 mL
    MICROASCUS BREVICAULIS (UNII: DHI513VXU7) (MICROASCUS BREVICAULIS - UNII:DHI513VXU7) MICROASCUS BREVICAULIS0.0036 g  in 1 mL
    COLLETOTRICHUM COCCODES (UNII: Y0M7LGE3Z8) (COLLETOTRICHUM COCCODES - UNII:Y0M7LGE3Z8) COLLETOTRICHUM COCCODES0.0036 g  in 1 mL
    PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (PLEOSPORA HERBARUM - UNII:0N3Z1P4B2W) PLEOSPORA HERBARUM0.0036 g  in 1 mL
    STREPTOMYCES GRISEUS (UNII: G0O5980Z7W) (STREPTOMYCES GRISEUS - UNII:G0O5980Z7W) STREPTOMYCES GRISEUS0.0036 g  in 1 mL
    TRICHODERMA VIRIDE (UNII: T8678F0P0Q) (TRICHODERMA VIRIDE - UNII:T8678F0P0Q) TRICHODERMA VIRIDE0.0036 g  in 1 mL
    TRICHOPHYTON SCHOENLEINII (UNII: Z4MD1809H1) (TRICHOPHYTON SCHOENLEINII - UNII:Z4MD1809H1) TRICHOPHYTON SCHOENLEINII0.0036 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0036-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0036-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0036-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0036-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0036-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    A MOLD MIXTURE 
    a mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0005
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0008 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0008 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0008 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0008 g  in 1 mL
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.0033 g  in 1 mL
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.0033 g  in 1 mL
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.0033 g  in 1 mL
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.0033 g  in 1 mL
    GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.0033 g  in 1 mL
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0033 g  in 1 mL
    CANDIDA TROPICALIS (UNII: Q222J2186W) (CANDIDA TROPICALIS - UNII:Q222J2186W) CANDIDA TROPICALIS0.0017 g  in 1 mL
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.0017 g  in 1 mL
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0011 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.0011 g  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0006 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0006 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0006 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0006 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0006 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0006 g  in 1 mL
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.0033 g  in 1 mL
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0033 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0033 g  in 1 mL
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA0.0033 g  in 1 mL
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.0033 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0011 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0005-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0005-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0005-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0005-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0005-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PENICILLIUM NOTATUM 
    penicillium notatum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0417
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0417-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0417-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0417-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0417-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0417-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MUCOR MIXTURE 
    mucor mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0295
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0167 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.0167 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0167 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0295-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0295-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0295-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0295-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0295-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    A MOLD MIXTURE 
    a mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0006
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0004 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0004 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0004 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0004 g  in 1 mL
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.0017 g  in 1 mL
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.0017 g  in 1 mL
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.0017 g  in 1 mL
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.0017 g  in 1 mL
    GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.0017 g  in 1 mL
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.0017 g  in 1 mL
    CANDIDA TROPICALIS (UNII: Q222J2186W) (CANDIDA TROPICALIS - UNII:Q222J2186W) CANDIDA TROPICALIS0.0008 g  in 1 mL
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.0008 g  in 1 mL
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.0006 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.0006 g  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0003 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0003 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0003 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0003 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0003 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0003 g  in 1 mL
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.0017 g  in 1 mL
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.0017 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0017 g  in 1 mL
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA0.0017 g  in 1 mL
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.0017 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.0006 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0006-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0006-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0006-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0006-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0006-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON MIXTURE 
    trichophyton mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0577
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.025 g  in 1 mL
    TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0577-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0577-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0577-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0577-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0577-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PENICILLIUM MIXTURE 
    penicillium mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0364
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0083 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0083 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0083 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0083 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0083 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0083 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0364-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0364-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0364-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0364-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0364-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NUMBER TEN MOLD MIXTURE 
    number ten mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0587
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.005 g  in 1 mL
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0013 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0013 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0013 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0013 g  in 1 mL
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.005 g  in 1 mL
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.005 g  in 1 mL
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.005 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.005 g  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.0008 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0008 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.0008 g  in 1 mL
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.0008 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.0008 g  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.0008 g  in 1 mL
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.005 g  in 1 mL
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.005 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0587-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0587-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0587-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0587-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0587-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON MIXTURE 
    trichophyton mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0578
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.01 g  in 1 mL
    TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0578-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0578-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0578-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0578-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0578-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PHOMA 
    phoma injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0366
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0366-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0366-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0366-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0366-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0366-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NIGROSPORA 
    nigrospora injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0328
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0328-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0328-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0328-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0328-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0328-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PULLULARIA 
    pullularia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0369
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0369-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0369-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0369-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0369-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0369-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PULLULARIA 
    pullularia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0368
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0368-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0368-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0368-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0368-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0368-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0313
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0313-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0313-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0313-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0313-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0313-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MYCOGONE PERNICIOSA 
    mycogone perniciosa injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0297
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U) HYPOMYCES PERNICIOSUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0297-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0297-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0297-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0297-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0297-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MUCOR RACEMOSUS 
    mucor racemosus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0319
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0319-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0319-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0319-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0319-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0319-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0314
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0314-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0314-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0314-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0314-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0314-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHODERMA 
    trichoderma injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0563
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHODERMA VIRIDE (UNII: T8678F0P0Q) (TRICHODERMA VIRIDE - UNII:T8678F0P0Q) TRICHODERMA VIRIDE0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0563-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0563-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0563-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0563-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0563-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    STACHYBOTRYS 
    stachybotrys injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0471
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (STACHYBOTRYS CHARTARUM - UNII:HJ4L70T1ZP) STACHYBOTRYS CHARTARUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0471-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0471-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0471-35 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0471-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0471-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ASPERGILLUS MIXTURE 
    aspergillus mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0008
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.0125 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.0125 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.0125 g  in 1 mL
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.0125 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0008-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0008-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0008-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0008-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0008-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON RUBRUM 
    trichophyton rubrum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0580
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0580-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0580-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0580-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0580-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0580-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    RHIZOPUS 
    rhizopus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0435
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0435-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0435-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0435-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0435-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0435-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PAECILOMYCES 
    paecilomyces injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0371
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0025 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0371-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0371-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0371-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0371-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0371-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    STEMPHYLIUM 
    stemphylium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0467
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (PLEOSPORA HERBARUM - UNII:0N3Z1P4B2W) PLEOSPORA HERBARUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0467-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0467-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0467-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0467-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0467-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    SPONDYLOCLADIUM 
    spondylocladium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0465
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COLLETOTRICHUM COCCODES (UNII: Y0M7LGE3Z8) (COLLETOTRICHUM COCCODES - UNII:Y0M7LGE3Z8) COLLETOTRICHUM COCCODES0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0465-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0465-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0465-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0465-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0465-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    WHEAT SMUT 
    wheat smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0607
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    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) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0607-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0607-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0607-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0607-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0607-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222309/09/1997
    GLIOCLADIUM 
    gliocladium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0217
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MYROTHECIUM VERRUCARIA (UNII: W5U19AK212) (MYROTHECIUM VERRUCARIA - UNII:W5U19AK212) MYROTHECIUM VERRUCARIA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0217-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0217-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0217-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0217-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0217-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    FUSARIUM OXYSPORUM 
    fusarium oxysporum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0197
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (FUSARIUM OXYSPORUM - UNII:5398RXP8KU) FUSARIUM OXYSPORUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0197-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0197-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0197-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0197-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0197-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    HORMODENDRUM 
    hormodendrum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0244
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0244-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0244-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0244-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0244-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0244-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    GEOTRICHUM CANDIDUM 
    geotrichum candidum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0228
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (GEOTRICHUM CANDIDUM - UNII:5964J742O8) GEOTRICHUM CANDIDUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0228-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0228-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0228-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0228-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0228-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CLADOSPORIUM HERBARUM 
    cladosporium herbarum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0158
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM HERBARUM (UNII: O64JF11198) (CLADOSPORIUM HERBARUM - UNII:O64JF11198) CLADOSPORIUM HERBARUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0158-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0158-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0158-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0158-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0158-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    CORN SMUT 
    corn smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0143
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    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) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0143-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0143-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0143-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0143-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0143-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222309/09/1977
    EPIDERMOPHYTON 
    epidermophyton injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0194
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S) EPIDERMOPHYTON FLOCCOSUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0194-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0194-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0194-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0194-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0194-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    EPICOCCUM 
    epicoccum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0186
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0186-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0186-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0186-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0186-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0186-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0312
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0312-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0312-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0312-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0312-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0312-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    CANDIDA TROPICALIS 
    candida tropicalis injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0320
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA TROPICALIS (UNII: Q222J2186W) (CANDIDA TROPICALIS - UNII:Q222J2186W) CANDIDA TROPICALIS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0320-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0320-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0320-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0320-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0320-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MUCOR RACEMOSUS 
    mucor racemosus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0318
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0318-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0318-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0318-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0318-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0318-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    JOHNSON GRASS SMUT 
    johnson grass smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0278
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0278-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0278-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0278-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0278-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0278-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    HELMINTHOSPORIUM 
    helminthosporium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0247
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0247-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0247-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0247-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0247-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0247-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    MICROSPORUM AUDOUINII 
    microsporum audouinii injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0298
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICROSPORUM AUDOUINII (UNII: B7B86Y84R8) (MICROSPORUM AUDOUINII - UNII:B7B86Y84R8) MICROSPORUM AUDOUINII0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0298-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0298-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0298-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0298-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0298-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MYCOGONE PERNICIOSA 
    mycogone perniciosa injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0296
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOMYCES PERNICIOSUS (UNII: 6K41G30A6U) (HYPOMYCES PERNICIOSUS - UNII:6K41G30A6U) HYPOMYCES PERNICIOSUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0296-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0296-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0296-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0296-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0296-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0030
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0030-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0030-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0030-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0030-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0030-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    ASPERGILLUS REPENS 
    aspergillus repens injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0621
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS REPENS (UNII: SQ89E6LOME) (ASPERGILLUS REPENS - UNII:SQ89E6LOME) ASPERGILLUS REPENS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0621-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0621-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0621-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0621-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0621-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ASPERGILLUS NIGER 
    aspergillus niger injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0032
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0032-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0032-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0032-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0032-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0032-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    ASPERGILLUS FLAVUS 
    aspergillus flavus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0624
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (ASPERGILLUS FLAVUS - UNII:3J888Y9L13) ASPERGILLUS FLAVUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0624-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0624-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0624-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0624-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0624-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON SCHOENLEINII 
    trichophyton schoenleinii injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0618
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON SCHOENLEINII (UNII: Z4MD1809H1) (TRICHOPHYTON SCHOENLEINII - UNII:Z4MD1809H1) TRICHOPHYTON SCHOENLEINII0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0618-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0618-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0618-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0618-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0618-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ALTERNARIA ALTERNATA 
    alternaria alternata injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0001
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0001-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0001-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0001-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0001-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0001-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    ACROTHECIUM ROBUSTUM 
    acrothecium robustum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0620
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACROTHECIUM ROBUSTUM (UNII: C91ZMT66YA) (ACROTHECIUM ROBUSTUM - UNII:C91ZMT66YA) ACROTHECIUM ROBUSTUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0620-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0620-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0620-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0620-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0620-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    ABSIDIA RAMOSA 
    absidia ramosa injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0619
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MYCOCLADUS CORYMBIFERUS (UNII: 1M4E76V32I) (MYCOCLADUS CORYMBIFERUS - UNII:1M4E76V32I) MYCOCLADUS CORYMBIFERUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0619-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0619-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0619-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0619-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0619-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CEPHALOTHECIUM 
    cephalothecium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0095
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOTHECIUM ROSEUM (UNII: TGO054E31O) (TRICHOTHECIUM ROSEUM - UNII:TGO054E31O) TRICHOTHECIUM ROSEUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0095-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0095-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0095-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0095-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0095-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    CHAETOMIUM 
    chaetomium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0093
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0093-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0093-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0093-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0093-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0093-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    CURVULARIA 
    curvularia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0097
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0097-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0097-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0097-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0097-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0097-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    CLADOSPORIUM FULVUM 
    cladosporium fulvum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0096
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASSALORA FULVA (UNII: HR6H5057CO) (PASSALORA FULVA - UNII:HR6H5057CO) PASSALORA FULVA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0096-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0096-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0096-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0096-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0096-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    BERMUDA GRASS SMUT 
    bermuda grass smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0064
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO CYNODONTIS (UNII: 0V3J4YEX2W) (USTILAGO CYNODONTIS - UNII:0V3J4YEX2W) USTILAGO CYNODONTIS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0064-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0064-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0064-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0064-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0064-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    BOTRYTIS 
    botrytis injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0038
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0038-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0038-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0038-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0038-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0038-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    CEPHALOSPORIUM 
    cephalosporium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0087
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0087-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0087-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0087-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0087-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0087-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    BARLEY SMUT 
    barley smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0066
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO NUDA HORDEI (UNII: 9Y53ZS6I82) (USTILAGO NUDA HORDEI - UNII:9Y53ZS6I82) USTILAGO NUDA HORDEI0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0066-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0066-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0066-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0066-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0066-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    SPONDYLOCLADIUM 
    spondylocladium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0464
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COLLETOTRICHUM COCCODES (UNII: Y0M7LGE3Z8) (COLLETOTRICHUM COCCODES - UNII:Y0M7LGE3Z8) COLLETOTRICHUM COCCODES0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0464-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0464-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0464-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0464-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0464-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    SCOPULARIOPSIS 
    scopulariopsis injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0463
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICROASCUS BREVICAULIS (UNII: DHI513VXU7) (MICROASCUS BREVICAULIS - UNII:DHI513VXU7) MICROASCUS BREVICAULIS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0463-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0463-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0463-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0463-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0463-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    STREPTOMYCES 
    streptomyces injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0468
    Route of AdministrationSUBCONJUNCTIVAL, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STREPTOMYCES GRISEUS (UNII: G0O5980Z7W) (STREPTOMYCES GRISEUS - UNII:G0O5980Z7W) STREPTOMYCES GRISEUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0468-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0468-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0468-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0468-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0468-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    STEMPHYLIUM 
    stemphylium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0466
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (PLEOSPORA HERBARUM - UNII:0N3Z1P4B2W) PLEOSPORA HERBARUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0466-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0466-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0466-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0466-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0466-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    RHIZOPUS 
    rhizopus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0434
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0434-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0434-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0434-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0434-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0434-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    PENICILLIUM ITALICUM 
    penicillium italicum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0651
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM ITALICUM (UNII: AZJ5XKM7W3) (PENICILLIUM ITALICUM - UNII:AZJ5XKM7W3) PENICILLIUM ITALICUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0651-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0651-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0651-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0651-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0651-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    SACCHAROMYCES 
    saccharomyces injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0462
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0462-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0462-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0462-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0462-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0462-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    RHODOTORULA 
    rhodotorula injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0436
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0436-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0436-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0436-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0436-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0436-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON RUBRUM 
    trichophyton rubrum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0579
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0579-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0579-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0579-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0579-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0579-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    TETRACOCCOSPORIUM PAXIANUM 
    tetracoccosporium paxianum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0564
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TETRACOCCOSPORIUM PAXIANUM (UNII: KSY1AWN59I) (TETRACOCCOSPORIUM PAXIANUM - UNII:KSY1AWN59I) TETRACOCCOSPORIUM PAXIANUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0564-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0564-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0564-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0564-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0564-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    VERTICILLIUM 
    verticillium injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0594
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VERTICILLIUM ALBO-ATRUM (UNII: X92O101CS2) (VERTICILLIUM ALBO-ATRUM - UNII:X92O101CS2) VERTICILLIUM ALBO-ATRUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0594-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0594-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0594-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0594-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0594-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0585
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0585-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0585-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0585-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0585-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0585-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    STACHYBOTRYS 
    stachybotrys injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0470
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (STACHYBOTRYS CHARTARUM - UNII:HJ4L70T1ZP) STACHYBOTRYS CHARTARUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0470-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0470-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0470-35 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0470-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0470-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    SPOROTRICHUM 
    sporotrichum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0469
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SPOROTRICHUM PRUINOSUM (UNII: H20KU95UBG) (SPOROTRICHUM PRUINOSUM - UNII:H20KU95UBG) SPOROTRICHUM PRUINOSUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0469-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0469-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0469-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0469-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0469-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    TRICHODERMA 
    trichoderma injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0562
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHODERMA VIRIDE (UNII: T8678F0P0Q) (TRICHODERMA VIRIDE - UNII:T8678F0P0Q) TRICHODERMA VIRIDE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0562-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0562-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0562-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0562-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0562-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    SYNCEPHALASTRUM 
    syncephalastrum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0472
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SYNCEPHALASTRUM RACEMOSUM (UNII: 2VWV12V9WR) (SYNCEPHALASTRUM RACEMOSUM - UNII:2VWV12V9WR) SYNCEPHALASTRUM RACEMOSUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0472-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0472-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0472-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0472-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0472-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    OAT SMUT 
    oat smut injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0342
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO AVENAE (UNII: YIH315U1TU) (USTILAGO AVENAE - UNII:YIH315U1TU) USTILAGO AVENAE0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0342-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0342-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0342-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0342-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0342-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NIGROSPORA 
    nigrospora injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0327
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0327-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0327-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0327-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0327-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0327-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    PULLULARIA 
    pullularia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0367
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0367-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0367-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0367-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0367-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0367-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    PHOMA 
    phoma injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0365
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA DESTRUCTIVA (UNII: A17SE577FM) (PHOMA DESTRUCTIVA - UNII:A17SE577FM) PHOMA DESTRUCTIVA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0365-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0365-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0365-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0365-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0365-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    MUCOR MUCEDO 
    mucor mucedo injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0637
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0637-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0637-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0637-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0637-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0637-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0326
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0326-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0326-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0326-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0326-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0326-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    NEUROSPORA CRASSA 
    neurospora crassa injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0639
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NEUROSPORA CRASSA (UNII: 1X92VM01YP) (NEUROSPORA CRASSA - UNII:1X92VM01YP) NEUROSPORA CRASSA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0639-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0639-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0639-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0639-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0639-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0638
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0638-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0638-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0638-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0638-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0638-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PENICILLIUM CAMEMBERTII 
    penicillium camembertii injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0648
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (PENICILLIUM CAMEMBERTI - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0648-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0648-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0648-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0648-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0648-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PENICILLIUM ROQUEFORTII 
    penicillium roquefortii injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0647
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0647-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0647-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0647-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0647-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0647-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PENICILLIUM EXPANSUM 
    penicillium expansum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0650
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0650-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0650-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0650-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0650-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0650-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PENICILLIUM CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0649
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0649-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0649-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0649-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0649-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0649-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PAPULARIA 
    papularia injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0372
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    APIOSPORA MONTAGNEI (UNII: 49VI1ZSO06) (APIOSPORA MONTAGNEI - UNII:49VI1ZSO06) APIOSPORA MONTAGNEI0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0372-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0372-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0372-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0372-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0372-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    PAECILOMYCES 
    paecilomyces injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0370
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (PAECILOMYCES VARIOTII - UNII:KO7V58BY40) PAECILOMYCES VARIOTII0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0370-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0370-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0370-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0370-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0370-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    PENICILLIUM NOTATUM 
    penicillium notatum injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0416
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0416-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0416-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0416-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0416-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0416-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    PHYCOMYCES 
    phycomyces injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0373
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHYCOMYCES BLAKESLEEANUS (UNII: 41Y752Y34M) (PHYCOMYCES BLAKESLEEANUS - UNII:41Y752Y34M) PHYCOMYCES BLAKESLEEANUS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0373-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0373-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0373-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0373-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0373-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    HUMICOLA GRISEA 
    humicola grisea injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0635
    Route of AdministrationINTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HUMICOLA GRISEA (UNII: RZ55S3AQOJ) (HUMICOLA GRISEA - UNII:RZ55S3AQOJ) HUMICOLA GRISEA0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0635-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0635-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0635-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0635-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0635-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    C MOLD MIXTURE 
    c mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0090
    Route of AdministrationINTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MYCOCLADUS CORYMBIFERUS (UNII: 1M4E76V32I) (MYCOCLADUS CORYMBIFERUS - UNII:1M4E76V32I) MYCOCLADUS CORYMBIFERUS0.0083 g  in 1 mL
    ACROTHECIUM ROBUSTUM (UNII: C91ZMT66YA) (ACROTHECIUM ROBUSTUM - UNII:C91ZMT66YA) ACROTHECIUM ROBUSTUM0.0083 g  in 1 mL
    HUMICOLA GRISEA (UNII: RZ55S3AQOJ) (HUMICOLA GRISEA - UNII:RZ55S3AQOJ) HUMICOLA GRISEA0.0083 g  in 1 mL
    MICROSPORUM AUDOUINII (UNII: B7B86Y84R8) (MICROSPORUM AUDOUINII - UNII:B7B86Y84R8) MICROSPORUM AUDOUINII0.0083 g  in 1 mL
    MICROSPORUM CANIS (UNII: N4F4RQ7BY7) (MICROSPORUM CANIS - UNII:N4F4RQ7BY7) MICROSPORUM CANIS0.0083 g  in 1 mL
    APIOSPORA MONTAGNEI (UNII: 49VI1ZSO06) (APIOSPORA MONTAGNEI - UNII:49VI1ZSO06) APIOSPORA MONTAGNEI0.0083 g  in 1 mL
    PHYCOMYCES BLAKESLEEANUS (UNII: 41Y752Y34M) (PHYCOMYCES BLAKESLEEANUS - UNII:41Y752Y34M) PHYCOMYCES BLAKESLEEANUS0.0083 g  in 1 mL
    SPOROTRICHUM PRUINOSUM (UNII: H20KU95UBG) (SPOROTRICHUM PRUINOSUM - UNII:H20KU95UBG) SPOROTRICHUM PRUINOSUM0.0083 g  in 1 mL
    STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (STACHYBOTRYS CHARTARUM - UNII:HJ4L70T1ZP) STACHYBOTRYS CHARTARUM0.0083 g  in 1 mL
    SYNCEPHALASTRUM RACEMOSUM (UNII: 2VWV12V9WR) (SYNCEPHALASTRUM RACEMOSUM - UNII:2VWV12V9WR) SYNCEPHALASTRUM RACEMOSUM0.0083 g  in 1 mL
    TETRACOCCOSPORIUM PAXIANUM (UNII: KSY1AWN59I) (TETRACOCCOSPORIUM PAXIANUM - UNII:KSY1AWN59I) TETRACOCCOSPORIUM PAXIANUM0.0083 g  in 1 mL
    VERTICILLIUM ALBO-ATRUM (UNII: X92O101CS2) (VERTICILLIUM ALBO-ATRUM - UNII:X92O101CS2) VERTICILLIUM ALBO-ATRUM0.0083 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0090-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0090-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0090-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0090-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0090-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222304/13/1992
    C MOLD MIXTURE 
    c mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0091
    Route of AdministrationINTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MYCOCLADUS CORYMBIFERUS (UNII: 1M4E76V32I) (MYCOCLADUS CORYMBIFERUS - UNII:1M4E76V32I) MYCOCLADUS CORYMBIFERUS0.0042 g  in 1 mL
    ACROTHECIUM ROBUSTUM (UNII: C91ZMT66YA) (ACROTHECIUM ROBUSTUM - UNII:C91ZMT66YA) ACROTHECIUM ROBUSTUM0.0042 g  in 1 mL
    HUMICOLA GRISEA (UNII: RZ55S3AQOJ) (HUMICOLA GRISEA - UNII:RZ55S3AQOJ) HUMICOLA GRISEA0.0042 g  in 1 mL
    MICROSPORUM AUDOUINII (UNII: B7B86Y84R8) (MICROSPORUM AUDOUINII - UNII:B7B86Y84R8) MICROSPORUM AUDOUINII0.0042 g  in 1 mL
    MICROSPORUM CANIS (UNII: N4F4RQ7BY7) (MICROSPORUM CANIS - UNII:N4F4RQ7BY7) MICROSPORUM CANIS0.0042 g  in 1 mL
    APIOSPORA MONTAGNEI (UNII: 49VI1ZSO06) (APIOSPORA MONTAGNEI - UNII:49VI1ZSO06) APIOSPORA MONTAGNEI0.0042 g  in 1 mL
    PHYCOMYCES BLAKESLEEANUS (UNII: 41Y752Y34M) (PHYCOMYCES BLAKESLEEANUS - UNII:41Y752Y34M) PHYCOMYCES BLAKESLEEANUS0.0042 g  in 1 mL
    SPOROTRICHUM PRUINOSUM (UNII: H20KU95UBG) (SPOROTRICHUM PRUINOSUM - UNII:H20KU95UBG) SPOROTRICHUM PRUINOSUM0.0042 g  in 1 mL
    STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (STACHYBOTRYS CHARTARUM - UNII:HJ4L70T1ZP) STACHYBOTRYS CHARTARUM0.0042 g  in 1 mL
    SYNCEPHALASTRUM RACEMOSUM (UNII: 2VWV12V9WR) (SYNCEPHALASTRUM RACEMOSUM - UNII:2VWV12V9WR) SYNCEPHALASTRUM RACEMOSUM0.0042 g  in 1 mL
    TETRACOCCOSPORIUM PAXIANUM (UNII: KSY1AWN59I) (TETRACOCCOSPORIUM PAXIANUM - UNII:KSY1AWN59I) TETRACOCCOSPORIUM PAXIANUM0.0042 g  in 1 mL
    VERTICILLIUM ALBO-ATRUM (UNII: X92O101CS2) (VERTICILLIUM ALBO-ATRUM - UNII:X92O101CS2) VERTICILLIUM ALBO-ATRUM0.0042 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0091-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0091-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0091-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0091-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0091-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    C MOLD MIXTURE 
    c mold mixture injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49288-0092
    Route of AdministrationINTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MYCOCLADUS CORYMBIFERUS (UNII: 1M4E76V32I) (MYCOCLADUS CORYMBIFERUS - UNII:1M4E76V32I) MYCOCLADUS CORYMBIFERUS0.0021 g  in 1 mL
    ACROTHECIUM ROBUSTUM (UNII: C91ZMT66YA) (ACROTHECIUM ROBUSTUM - UNII:C91ZMT66YA) ACROTHECIUM ROBUSTUM0.0021 g  in 1 mL
    HUMICOLA GRISEA (UNII: RZ55S3AQOJ) (HUMICOLA GRISEA - UNII:RZ55S3AQOJ) HUMICOLA GRISEA0.0021 g  in 1 mL
    MICROSPORUM AUDOUINII (UNII: B7B86Y84R8) (MICROSPORUM AUDOUINII - UNII:B7B86Y84R8) MICROSPORUM AUDOUINII0.0021 g  in 1 mL
    MICROSPORUM CANIS (UNII: N4F4RQ7BY7) (MICROSPORUM CANIS - UNII:N4F4RQ7BY7) MICROSPORUM CANIS0.0021 g  in 1 mL
    APIOSPORA MONTAGNEI (UNII: 49VI1ZSO06) (APIOSPORA MONTAGNEI - UNII:49VI1ZSO06) APIOSPORA MONTAGNEI0.0021 g  in 1 mL
    PHYCOMYCES BLAKESLEEANUS (UNII: 41Y752Y34M) (PHYCOMYCES BLAKESLEEANUS - UNII:41Y752Y34M) PHYCOMYCES BLAKESLEEANUS0.0021 g  in 1 mL
    SPOROTRICHUM PRUINOSUM (UNII: H20KU95UBG) (SPOROTRICHUM PRUINOSUM - UNII:H20KU95UBG) SPOROTRICHUM PRUINOSUM0.0021 g  in 1 mL
    STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (STACHYBOTRYS CHARTARUM - UNII:HJ4L70T1ZP) STACHYBOTRYS CHARTARUM0.0021 g  in 1 mL
    SYNCEPHALASTRUM RACEMOSUM (UNII: 2VWV12V9WR) (SYNCEPHALASTRUM RACEMOSUM - UNII:2VWV12V9WR) SYNCEPHALASTRUM RACEMOSUM0.0021 g  in 1 mL
    TETRACOCCOSPORIUM PAXIANUM (UNII: KSY1AWN59I) (TETRACOCCOSPORIUM PAXIANUM - UNII:KSY1AWN59I) TETRACOCCOSPORIUM PAXIANUM0.0021 g  in 1 mL
    VERTICILLIUM ALBO-ATRUM (UNII: X92O101CS2) (VERTICILLIUM ALBO-ATRUM - UNII:X92O101CS2) VERTICILLIUM ALBO-ATRUM0.0021 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.525 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0095 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.0024 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49288-0092-12 mL in 1 VIAL, MULTI-DOSE
    2NDC:49288-0092-25 mL in 1 VIAL, MULTI-DOSE
    3NDC:49288-0092-310 mL in 1 VIAL, MULTI-DOSE
    4NDC:49288-0092-430 mL in 1 VIAL, MULTI-DOSE
    5NDC:49288-0092-550 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10222303/23/1974
    Labeler - Antigen Laboratories, Inc. (030705628)
    Registrant - Antigen Laboratories, Inc. (030705628)
    Establishment
    NameAddressID/FEIBusiness Operations
    Antigen Laboratories, Inc.030705628manufacture