Label: COTTONSEED injection
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DES .......ction
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COTTON LINTERS injection

  • NDC Code(s): 49643-003-05, 49643-003-10, 49643-003-30, 49643-003-50, view more
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  • Packager: Allermed Laboratories, Inc.
  • Category: NON-STANDARDIZED ALLERGENIC LABEL
  • DEA Schedule: None
  • Marketing Status: Biologic Licensing Application

Drug Label Information

Updated September 17, 2019

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

  • BOXED WARNING (What is this?)

    WARNINGS

    This allergenic product is intended for use by physicians who are experienced in the administration of allergenic extracts, and the emergency care of anaphylaxis, or for use under the guidance of an allergy specialist.
    This allergenic 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 being switched from other types of extracts, such as alum precipitated extracts, should be started as though they were coming under treatment for the first time. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician's office if reaction symptoms occur. As with all allergenic extracts, severe systemic reactions may occur. In certain individuals these systemic reactions may occur. In certain individuals these reactions may be life threatening. Patients should be observed for at least 20 minutes following treatment, and emergency measures as well as personnel trained in their use should be immediately available in the event of a life threatening reaction.
    This product should not be injected intravenously (see Dosage and Administration). Refer also to the Warnings, Precautions, Adverse Reactions and Overdosage sections below.

  • DESCRIPTION

    Allergenic extract contains the aqueous extractables from allergenic source material in extracting solution containing 0.25% sodium chloride, 0.125% sodium bicarbonate, and 50% glycerol. 0.4% phenol is added as a preservative. The weight by volume value shown on the label is a measurement of extract concentration, rather than extract potency. Extracts for which U.S. standards exist are labeled in allergy units, in addition to w/v strength.

  • CLINICAL PHARMACOLOGY

    Positive skin tests with allergenic extract are the result of histamine release from mast cells sensitized with allergen specific IgE. The exact mechanisms by which immunotherapy relieves symptoms of allergy are still under investigation. Elevations in allergen-specific IgG antibodies and an increase in the activity of T suppressor lymphocytes appear to be some of the immunologic changes that occur from hyposensitization. 1,2,3

  • INDICATIONS AND USAGE

    Allergenic extract may be used as a diagnostic skin test reagent in persons suspected of being sensitive to the allergenic source material from which the extract is made. Skin tests should be used in conjunction with a thorough allergic history to establish the relevance of a given allergen in the etiology of allergic disease. 4,5,6
    Immunotherapy with allergenic extract is indicated in persons suffering from allergic rhinitis, bronchitis, conjunctivitis, urticaria and asthma. The therapeutic efficacy of allergenic extract has been proven in ragweed, grass, and mountain cedar pollinosis, cat-induced asthma and hypersensitivity to hymenoptera venoms. 7-12
    Immunotherapy may be used along with or exclusive of antihistamines and other medications used to control allergic symptoms.

  • CONTRAINDICATIONS

    Allergenic extract should not be administered to a non-allergic person. However, there are no absolute contraindications to the use of allergenic extract for treatment in appropriate individuals. Relative contraindications include: EXTREME SENSITIVITY TO AN ALLERGEN - Determined from the allergic history, or from previous anaphylaxis following skin testing or subcutaneous injection; AUTOIMMUNE DISEASE - Individuals with autoimmune disease may be at risk, due to the possibility of routine immunizations exacerbating symptoms of the underlying disease; PREGNANCY - In limited controlled studies of women receiving allergenic extract during conception and throughout all trimesters of pregnancy, no evidence was found that extract is harmful to the fetus or mother. However, because of the known pharmacologic action of histamine on uterine muscle, any treatment that might result in the release of significant amounts of this mediator should be avoided if possible 13. See Precaution #4; MYOCARDIAL INFARCTION - Patients who have experienced a recent myocardial infarction may not be able to tolerate immunotherapy. As in all of the above circumstances, the benefit to risk ration must be carefully evaluated; BLEEDING DIATHESIS - Patients with a bleeding tendency should not be tested or treated with allergenic extract, unless the physician responsible believes that such procedures are safe to perform.
    Allergenic extract should be temporarily withheld from patients if any of the following conditions exist: (1) severe symptoms of hay fever and/or asthma; (2) infection or flu accompanied by fever; and (3) exposure to excessive amounts of clinically relevant allergens prior to skin testing or immunotherapy.

  • WARNINGS

    The only approved method for determining hypersensitivity to Allermed Laboratories Allergenic Extracts is by diagnostic skin testing (See DOSAGE AND ADMINISTRATION — DIAGNOSIS).
    Physicians who administer allergenic extract should have emergency medication and equipment available to treat anaphylaxis 14. See Precautions, Adverse Reactions and Overdosage below.
    To reduce the risk of anaphylaxis, the following measures must be observed:

    1. Concentrated extract must be diluted before use for intradermal skin testing and for beginning immunotherapy. It should never be injected intravenously during testing or treatment procedures.
    2. Patients who are highly sensitive, determined from clinical findings and test results, may require that treatment start with a very weak concentration of extract, such as 1:10,000,000 v/v.
    3. The dosage of fresh (new) extract given to a patient receiving maintenance injections must be reduced to one-fourth the amount given from the previous (old) lot (See Immunotherapy, last paragraph).
    4. Patients who are transferred to standardized extract after previous treatment with unstandardized extract must be skin tested with serial dilutions, starting with a 1:100,000 v/v dilution of the standardized extract, to determine a safe, non-reacting starting dose.
    5. Patients who are transferred to this extract after treatment with alum precipitated or other modified extract must re-start injections with the beginning recommended dose of this extract.
  • PRECAUTIONS

    1. Extract should be stored at 2°C to 8°C since higher temperatures may adversely affect the stability of the product. Do not freeze.
    2. After the needle is inserted subcutaneously, the plunger should be withdrawn slightly to check for the presence of blood in the syringe. If blood is observed, a new injection should be prepared and given at another site, observing the same precautions.
    3. Treatment with beta-blocking drugs may make patients refractory to the usual dose of epinephrine, in the event epinephrine is required to control an adverse allergic reaction.
    4. PREGNANCY CATEGORY C. Allergenic extract. Animal reproduction studies have not been conducted with allergenic extract. It is also not known whether allergenic extract can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Allergenic extract should be given to a pregnant woman only if clearly needed.
    5. PATIENT INSTRUCTIONS: Patients should be instructed to remain in the physician's office for at least 20 minutes after skin testing and after each treatment injection, and immediately notify the physician if symptoms of a generalized reaction or shock occur.
    6. CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: Long term studies have not been conducted with allergenic extracts to determine their potential for carcinogenesis, mutagenesis, and impairment of fertility.
    7. LACTATION: Data are not available on the secretion of allergenic extract in human milk and it is not known what affect this might have on the nursing infant.
    8. PEDIATRIC USE: The dose of allergenic extract recommended for children is the same as that used for adults, except in the injection of large doses of extract for treatment. In this case, the amount of extract given to a child may be modified so that the discomfort of the injection is minimized.
  • ADVERSE REACTIONS

    Local Reactions: The occurrence of a hive 5 to 15 minutes after the subcutaneous injection of extract does not require a reduction in dosage. However, a local reaction with edema larger than 2 cm in diameter or swelling and redness that persist for several hours or longer indicates that too much extract has been given. Treatment should be altered as follows:

    1. Additional injections should not be given until all evidence of the reaction has disappeared.
    2. The next injection administered should be 50% of the last non-reacting dose or less, depending upon the size and severity of the local reaction.
    3. Subsequent injections should be continued at the reduced dosage unless the physician responsible for treatment believes that it is safe to increase the dose, and that possible clinical improvement would result form the administration of a larger dose of extract.

    Systemic Reactions:Systemic (generalized) reactions may range from a mild exacerbation of the patient's allergic symptoms to hives, anaphylactic shock, or even death from anaphylaxis. The reaction usually occurs 5 to 20 minutes after injection. As a rule, the more quickly a reaction develops, the more serious it is likely to become. Symptoms may include sneezing, coughing, itching, shortness of breath, abdominal cramps, vomiting, diarrhea, tachycardia, hypotension and respiratory failure in severe cases. The reaction is usually stopped by the subcutaneous injection of Epinephrine HCL 1:1,000 (See Overdosage below). The oral administration of antihistamines and the placement of a tourniquet proximal to the injection site are helpful adjuncts. In the event that additional measures are required, it may be necessary to treat the patient for BRONCHOSPASM with intravenous aminophylline, intravenous fluids and corticosteroids; for HYPOTENSION with vasopressors, volume repletion, isoproterenol and corticosteroids; for LARYNGEAL OBSTRUCTION with oxygen and tracheostomy and for CARDIAC ARREST with cardiopulmonary resuscitation and other appropriate measures.
    Immunotherapy after anaphylaxis should be continued if the cause of the reaction can be identified and appropriate precautions taken to insure that a subsequent reaction does not occur.

  • OVERDOSAGE

    A strong local reaction to the injection of extract may be treated with oral antihistamines and the local application of a cold compress. The dosage must be reduced and additional extract must not be given until all evidence of the reaction has disappeared.
    A systemic reaction following the injection of extract must be treated immediately. Reported procedures include (Ref. #4, vol. 2, p. 888):

    1. 0.01 mL/kg up to 0.2 mL of aqueous epinephrine HCL 1:1000 subcutaneously at the injection site of antigen.
    2. 0.01 mL/kg up to 0.3 mL of aqueous epinephrine HCL 1:1000 subcutaneously at another site.
    3. Diphenhydramine intravenously or intramuscularly, 1.25 mg/kg up to 50 mg.
    4. Tourniquet above the injection site of antigen.

    Specific reactions:

    1. Brochospasm: intravenous aminophylline 4 mg/kg up to 500 mg given over 10 to 15 minutes, aqueous hydrocortisone 5 mg/kg up to 200 mg, oxygen.
    2. Laryngeal edema: oxygen, intubation, tracheostomy.
    3. Hypotension: vasopressors, fluids, corticosteroids.
    4. Cardiac arrest: resuscitation, sodium bicarbonate, defibrillation, antiarrhythmia medications.
  • DOSAGE AND ADMINISTRATION

    Diagnosis: Concentrated extract may be used for scratch or prick testing providing the patient is not extremely sensitive. In this case, the extract should be diluted 10 fold before a scratch or prick test is performed. Extract for intradermal testing must be used as follows:

    a. Patients with a negative scratch or prick test: Patients who do not react who do not react to a valid scratch or prick test should be tested intradermally with 0.05 mL of a 1:1000 v/v dilution of the concentrate. If the test is negative, a second test should be performed with 0.05 mL of a 1:100 v/v dilution or concentrate.
    b. Patients with positive scratch or prick tests: It is not advisable to perform an intradermal skin test if the patient has a positive scratch or prick test.
    c. Patients tested only by the intradermal method: Patients suspected of being highly allergic should be tested with 0.05 mL of a 1:100,000 v/v dilution of the concentrate. A negative test should be followed by repeat tests using 10 fold stronger concentrations until the maximum dose of 0.05 mL of a 1:100 v/v dilution is reached.

    Interpretation of Results
    Scratch and Prick Test
    A negative test shows only a slight red area at the site of scarification or prick penetration. Positive tests are scored as follows:

    1+ Erythema with 5 mm wheal
    2+ Erythema with a 5-10 mm wheal
    3+ Erythema with a 10-15 mm wheal
    4+ Erythema with a wheal 15 mm (or larger) with pseudopodia

    Intradermal Test
    A negative test shows no change in the appearance and size of the 5 mm wheal created by the I.D. injection of 0.05 mL of extract. Positive tests are scored as follows:

    1+ Erythema 10-20 mm with a 5-10 mm wheal
    2+ Erythema 20-30 mm with a 5-10 mm wheal
    3+ Erythema 30-40 mm with a 10-15 mm wheal
    4+ Erythema greater than 40 mm with a 15 mm wheal (or larger) with pseudopodia

    Immunotherapy

    Allergenic extract should be administered subcutaneously in the outer aspect of the upper arm using a sterile tuberculin syringe and needle. The skin should be cleaned with 70% alcohol and aseptic technique should be observed in removing the extract from the vial. Care must be taken to avoid injecting the extract into a blood vessel because of the risk of anaphylaxis.
    Concentrated extract must be diluted before administration to new patients. A 1:100,000 v/v dilution of concentrate is usually satisfactory to start treatment. However, as a precaution against overdose, a skin test with the intended starting dose should be done to help evaluate the patient's sensitivity to the product. If the skin response is larger than 5 mm edema/15 mm erythema, the extract is too strong and must be diluted before it is given subcutaneously. The doses shown in the Dosage Schedule (Table 1) below are recommended unless the patient's skin test response and allergic history indicates that more dilute extract should be used.
    Little is known about the required accumulated dosage of allergen that is needed to relieve symptoms. However, studies have shown that high dose immunotherapy is efficacious in the treatment of allergic rhinitis and asthma. For this reason, treatment with extract from Vial #5 is recommended, providing the patient can tolerate the extract without experiencing local or systemic reactions. Treatment with Vial #6 may be used for patients who have not had adverse reactions to extract in Vial #5 and who require more concentrated extract to control or relieve symptoms.
    Patients who have received allergenic extract for maintenance therapy SHOULD NOT be given the same dose from a fresh vial of extract. IT IS ADVISABLE TO REDUCE THE DOSAGE OF FRESH EXTRACT TO ONE-FOURTH THE AMOUNT GIVEN FROM A PREVIOUS LOT OF EXTRACT MADE AT THE SAME CONCENTRATION AND BY THE SAME FORMULA.

    Table 1 - Suggested Dosage Schedule
    No.
    Vial #1
    1:100,000 w/v
    frequency twice
    weekly
    mL
    Vial #2
    1:10,000 w/v
    frequency twice
    weekly
    mL
    Vial #3
    1:1,000 w/v
    frequency once
    weekly
    mL
    Vial #4
    1:100 w/v
    frequency once
    weekly
    mL
    Vial #5
    1:10 w/v
    frequency every
    two-four weeks
    mL
    Vial #6
    Concentrate
    frequency every
    two-four weeks
    mL
    1
    0.025
    0.025
    0.025
    0.025
    0.025
    0.025
    2
    0.05
    0.050.050.050.050.05
    3
    0.10
    0.10
    0.10
    0.10
    0.10
    0.10
    4
    0.15
    0.15
    0.15
    0.15
    0.15
    0.15
    5
    0.20
    0.20
    0.20
    0.20
    0.20
    0.20
    6
    0.25
    0.25
    0.25
    0.25
    0.25
    0.25
    7
    0.30
    0.30
    0.30
    0.30
    0.30
    0.30
  • SUPPLIED

    Allergenic extract is supplied in dropper vials for scratch or prick testing and in 10, 30, and 50 mL vials for bulk use.

    WARRANTY

    Allermed Laboratories, Inc. certifies that allergenic extract prepared within the Laboratories meets the safety and sterility standards of the F.D.A. Because the Laboratories have no control over the conditions under which extract is sued, or the purposes intended, neither a good nor a bad effect following its administration is warranted.
    The users of this product should be aware of the potential dangers involved in the injection of allergenic extract and accept the risk of any consequences resulting from such injections.
    No representatives of the Laboratories may change this warranty whether written, oral or implied. The buyer or user must assume full responsibility for the product after it leaves the premises of the Laboratories.

  • REFERENCES

    1. Levy, D.A., L.M., Lichtenstein, E.O. Goldstein and K. Ishizaka. Immunologic and cellular changes accompanying the therapy of pollen allergy. J. Clinical Investigations. 50:360, 1971.
    2. Evans, R., H. Pence, H. Kaplan and R. Rocklin. The effect of immunotherapy on humoral and cellular response in ragweed hayfever. J. Clinical Investigations. 57:1378, 1976.
    3. Ishizaka, K. Cellular events in the IgE antibody response. Adv. In Immunology. 23:50, 1976.
    4. Middleton, Elliott, Jr., C.E. Reed and E.F. Ellis (Eds.) Allergy, Principles and Practice Vols. 1&2, C.V. Mosby 1978.
    5. Sheldon, J.M., R.G. Lovell and K.P. Matthews. A Manual of Clinical Allergy. W.B. Saunders, 1967.
    6. Nelson, H.S. Diagnostic procedures in allergy. I. Allergy skin testing. Ann. Allergy. 51:411, 1983.
    7. Norma, P.S., W.L. Winkenwerder and L.M. Lichtenstein. Immunotherapy of hay fever with ragweed antigen E: comparisons with whole pollen extract and placebos. J. Allergy. 42:93, 1968.
    8. Milner, F.H. and E.C. Tees. Specific sensitivity to individual grass pollens in some hay fever patients. Clinical Allergy. 2:83, 1972.
    9. Frankland, A.W. and R. Augustine. Grass pollen antigens effective in treatment. Clinical Science. 23:95, 1962.
    10. Pence, H.L., D.Q. Mitchell, R.L. Greely, B.R. Updegraff and H.A. Selfridge. Immunotherapy for mountain cedar pollinosis: a double-blind controlled study. J. Allergy ad Clinical Immunology. 58:39, 1976.
    11. Taylor, W.W., J.L. Ohman, Jr. and F.C. Lowell. Immunotherapy in cat-induced asthma. Double-blind trial with evaluation of bronchial responses to cat allergen and histamine. J. Allergy and Clinical Immunology. 61:283. 1978.
    12. Lichtenstein, L.M., M.D. Valentine and A.K. Sobotka. Insect allergies. The state of the art. J. Allergy and Clinical Immunology. 61:268, 1978.
    13. Metzger, W.J., E. Turner and R. Patterson. The safety of immunotherapy during pregnancy. J. Allergy and Clinical Immunology. 61:268. 1978.
    14. Ouellette, J.J. Emergency management of allergic reactions. Modern Medicine 99, 1975.
  • Container Label

    Sample Container Label

  • INGREDIENTS AND APPEARANCE
    COTTONSEED 
    cottonseed injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-005
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COTTON SEED (UNII: DI0ZRJ0MXN) (COTTON SEED - UNII:DI0ZRJ0MXN) COTTON SEED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-005-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-005-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-005-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-005-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CULTIVATED OAT POLLEN 
    avena sativa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-322
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVENA SATIVA POLLEN (UNII: A7IKY24TR7) (AVENA SATIVA POLLEN - UNII:A7IKY24TR7) AVENA SATIVA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-322-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-322-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-322-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-322-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CURVULARIA 
    curvularia lunata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-109
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS LUNATUS (UNII: 4T82EA86AJ) (COCHLIOBOLUS LUNATUS - UNII:4T82EA86AJ) COCHLIOBOLUS LUNATUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-109-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-109-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-109-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-109-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CYPRESS, ARIZONA POLLEN 
    cupressus arizonica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-341
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF) CUPRESSUS ARIZONICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-341-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-341-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-341-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-341-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    DANDELION POLLEN 
    taraxacum officinale injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-416
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TARAXACUM OFFICINALE POLLEN (UNII: WQ3S5294XY) (TARAXACUM OFFICINALE POLLEN - UNII:WQ3S5294XY) TARAXACUM OFFICINALE POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-416-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-416-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-416-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-416-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    DATE PALM POLLEN 
    phoenix dactylifera injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-387
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOENIX DACTYLIFERA POLLEN (UNII: 2FV55IRB5B) (PHOENIX DACTYLIFERA POLLEN - UNII:2FV55IRB5B) PHOENIX DACTYLIFERA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-387-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-387-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-387-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-387-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    DESERT RAGWEED POLLEN 
    ambrosia dumosa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-355
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA DUMOSA POLLEN (UNII: ZIO18VN6HJ) (AMBROSIA DUMOSA POLLEN - UNII:ZIO18VN6HJ) AMBROSIA DUMOSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-355-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-355-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-355-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-355-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    DOCK, YELLOW POLLEN 
    rumex crispus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-406
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-406-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-406-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-406-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-406-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    DOG HAIR 
    dog hair injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-006
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (CANIS LUPUS FAMILIARIS HAIR - UNII:05S7L91ZTR) CANIS LUPUS FAMILIARIS HAIR0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-006-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-006-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-006-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-006-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    EASTERN COTTONWOOD POLLEN 
    populus deltoides injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-395
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-395-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-395-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-395-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-395-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    EASTERN SYCAMORE POLLEN 
    platanus occidentalis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-391
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-391-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-391-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-391-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-391-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    EASTERN WHITE PINE POLLEN 
    pinus strobus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-388
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PINUS STROBUS POLLEN (UNII: TX1ER5UV3T) (PINUS STROBUS POLLEN - UNII:TX1ER5UV3T) PINUS STROBUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-388-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-388-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-388-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-388-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ENGLISH PLANTAIN POLLEN 
    plantago lanceolata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-389
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-389-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-389-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-389-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-389-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ENGLISH WALNUT POLLEN 
    juglans regia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-367
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1) JUGLANS REGIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-367-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-367-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-367-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-367-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    EPICOCCUM 
    epicoccum nigrum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-110
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    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
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-110-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-110-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-110-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-110-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    EUCALYPTUS POLLEN 
    eucalyptus globulus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-347
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (EUCALYPTUS GLOBULUS POLLEN - UNII:7XW7TB10X9) EUCALYPTUS GLOBULUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-347-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-347-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-347-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-347-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    EUROPEAN OLIVE POLLEN 
    olea europea injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-383
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-383-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-383-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-383-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-383-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    FALSE RAGWEED POLLEN 
    ambrosia acanthicarpa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-351
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (AMBROSIA ACANTHICARPA POLLEN - UNII:U2AI3H2J5Y) AMBROSIA ACANTHICARPA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-351-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-351-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-351-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-351-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    FLAXSEED 
    flaxseed injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-010
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FLAX SEED (UNII: 4110YT348C) (FLAX SEED - UNII:4110YT348C) FLAX SEED0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-010-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-010-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-010-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-010-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    FREMONT COTTONWOOD POLLEN 
    populus fremontii injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-396
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS FREMONTII POLLEN (UNII: 426RHB4302) (POPULUS FREMONTII POLLEN - UNII:426RHB4302) POPULUS FREMONTII POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-396-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-396-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-396-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-396-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    FUSARIUM 
    fusarium solani injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-111
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (HAEMATONECTRIA HAEMATOCOCCA - UNII:7TLR512M4A) HAEMATONECTRIA HAEMATOCOCCA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-111-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-111-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-111-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-111-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GAMBELS OAK POLLEN 
    quercus gambelii injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-404
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS GAMBELII POLLEN (UNII: 9HC15X34LX) (QUERCUS GAMBELII POLLEN - UNII:9HC15X34LX) QUERCUS GAMBELII POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-404-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-404-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-404-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-404-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GIANT RAGWEED POLLEN 
    ambrosia trifida injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-317
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-317-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-317-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-317-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-317-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GLYCEROL-SALINE CONTROL 
    glycerol-saline diluent injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-818
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.53 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-818-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-818-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-818-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-818-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GOAT EPITHELIA 
    goat epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-011
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPRA HIRCUS SKIN (UNII: JLG9853E2P) (CAPRA HIRCUS SKIN - UNII:JLG9853E2P) CAPRA HIRCUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-011-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-011-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-011-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-011-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GRAMA GRASS POLLEN 
    bouteloua spp. injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-326
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOUTELOUA GRACILIS POLLEN (UNII: 2XO08315X1) (BOUTELOUA GRACILIS POLLEN - UNII:2XO08315X1) BOUTELOUA GRACILIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-326-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-326-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-326-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-326-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GRAY (WHITE) BIRCH POLLEN 
    betula populifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-325
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (BETULA POPULIFOLIA POLLEN - UNII:23H70FYJ5U) BETULA POPULIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-325-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-325-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-325-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-325-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GREASEWOOD POLLEN 
    sarcobatus vermiculatus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-411
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SARCOBATUS VERMICULATUS POLLEN (UNII: 6532U64A3X) (SARCOBATUS VERMICULATUS POLLEN - UNII:6532U64A3X) SARCOBATUS VERMICULATUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-411-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-411-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-411-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-411-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GREEN ASH POLLEN 
    fraxinus pennsylvanica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-358
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS PENNSYLVANICA POLLEN (UNII: 2WZG2G15WX) (FRAXINUS PENNSYLVANICA POLLEN - UNII:2WZG2G15WX) FRAXINUS PENNSYLVANICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-358-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-358-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-358-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-358-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    GUINEA PIG EPITHELIA 
    guinea pig epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-012
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-012-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-012-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-012-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-012-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HACKBERRY POLLEN 
    celtis occidentalis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-336
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (CELTIS OCCIDENTALIS POLLEN - UNII:68R9X9Y96X) CELTIS OCCIDENTALIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-336-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-336-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-336-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-336-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HAMSTER EPITHELIA 
    hamster epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-013
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MESOCRICETUS AURATUS SKIN (UNII: 3K873H631W) (MESOCRICETUS AURATUS SKIN - UNII:3K873H631W) MESOCRICETUS AURATUS SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-013-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-013-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-013-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-013-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HARD MAPLE POLLEN 
    acer saccharum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-452
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-452-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-452-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-452-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-452-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HAZELNUT POLLEN 
    corylus americana injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-340
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CORYLUS AMERICANA POLLEN (UNII: ZGS382Y3AV) (CORYLUS AMERICANA POLLEN - UNII:ZGS382Y3AV) CORYLUS AMERICANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-340-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-340-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-340-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-340-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HELMINTHOSPORIUM SATIVUM 
    helminthosporium sativum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-112
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-112-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-112-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-112-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-112-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HOG EPITHELIA 
    hog epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-014
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SUS SCROFA SKIN (UNII: 3EM4VW6TQN) (SUS SCROFA SKIN - UNII:3EM4VW6TQN) SUS SCROFA SKIN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-014-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-014-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-014-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-014-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HORSE EPITHELIA 
    horse epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-015
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-015-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-015-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-015-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-015-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    HOUSE DUST 
    house dust injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-008
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-008-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-008-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-008-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-008-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    IODINE BUSH POLLEN 
    allenrolfea occidentalis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-311
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI) (ALLENROLFEA OCCIDENTALIS POLLEN - UNII:5W6JAI84OI) ALLENROLFEA OCCIDENTALIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-311-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-311-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-311-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-311-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    JOHNSON GRASS POLLEN 
    sorghum halepense injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-413
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-413-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-413-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-413-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-413-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    JUTE 
    jute injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-016
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CORCORUS CAPSULARIS FIBER (UNII: TVA75O7S63) (CORCORUS CAPSULARIS FIBER - UNII:TVA75O7S63) CORCORUS CAPSULARIS FIBER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-016-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-016-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-016-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-016-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    KAPOK 
    kapok injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-017
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9) CEIBA PENTANDRA FIBER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-017-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-017-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-017-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-017-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    KARAYA GUM 
    karaya gum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-018
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KARAYA GUM (UNII: 73W9IQY50Q) (KARAYA GUM - UNII:73W9IQY50Q) KARAYA GUM0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-018-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-018-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-018-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-018-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    KOELERS GRASS POLLEN 
    koeleria cristata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-375
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KOELERIA MACRANTHA POLLEN (UNII: IIC6H3WF6J) (KOELERIA MACRANTHA POLLEN - UNII:IIC6H3WF6J) KOELERIA MACRANTHA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-375-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-375-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-375-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-375-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    LAMBS QUARTERS POLLEN 
    chenopodium album injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-339
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-339-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-339-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-339-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-339-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    LENS SCALE POLLEN 
    atriplex lentiformis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-440
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I) (ATRIPLEX LENTIFORMIS POLLEN - UNII:86LWA5503I) ATRIPLEX LENTIFORMIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-440-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-440-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-440-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-440-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    LINDEN POLLEN 
    tilia cordata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-460
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TILIA CORDATA POLLEN (UNII: OCO1LJR5YN) (TILIA CORDATA POLLEN - UNII:OCO1LJR5YN) TILIA CORDATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-460-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-460-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-460-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-460-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    LOMBARD POPLAR POLLEN 
    populus nigra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-397
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS NIGRA POLLEN (UNII: 0MGE63QPFJ) (POPULUS NIGRA POLLEN - UNII:0MGE63QPFJ) POPULUS NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-397-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-397-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-397-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-397-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MELALEUCA POLLEN 
    melaleuca leucadendron injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-380
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-380-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-380-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-380-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-380-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MESQUITE POLLEN 
    prosopis juliflora injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-400
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-400-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-400-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-400-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-400-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MONILIA 
    monilia sitophila injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-113
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHRYSONILIA SITOPHILA (UNII: 296FK85FY6) (CHRYSONILIA SITOPHILA - UNII:296FK85FY6) CHRYSONILIA SITOPHILA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-113-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-113-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-113-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-113-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MOUNTAIN CEDAR POLLEN 
    juniperus sabinoides injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-371
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-371-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-371-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-371-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-371-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MOUSE EPITHELIA 
    mouse epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-019
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-019-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-019-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-019-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-019-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MUCOR 
    mucor racemosus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-114
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    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
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-114-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-114-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-114-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-114-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MUGWORT SAGE POLLEN 
    artemisia vulgaris injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-321
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-321-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-321-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-321-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-321-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    MUSTARD POLLEN 
    brassica campestris injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-327
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BRASSICA RAPA POLLEN (UNII: 85Z8OHV3K7) (BRASSICA RAPA POLLEN - UNII:85Z8OHV3K7) BRASSICA RAPA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-327-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-327-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-327-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-327-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    NETTLE POLLEN 
    urtica dioica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-423
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (URTICA DIOICA POLLEN - UNII:DNB59M1NVU) URTICA DIOICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-423-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-423-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-423-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-423-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ORRIS ROOT 
    orris root injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-020
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD) (IRIS GERMANICA VAR. FLORENTINA ROOT - UNII:M30XO5X4XD) IRIS GERMANICA VAR. FLORENTINA ROOT0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-020-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-020-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-020-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-020-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PALO VERDE POLLEN 
    cercidium torreyana injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-338
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PARKINSONIA FLORIDA POLLEN (UNII: 57586C96ZL) (PARKINSONIA FLORIDA POLLEN - UNII:57586C96ZL) PARKINSONIA FLORIDA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-338-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-338-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-338-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-338-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PECAN POLLEN 
    carya illinoinensis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-444
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-444-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-444-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-444-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-444-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PENICILLIUM 
    penicillium chrysogenum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-115
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-115-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-115-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-115-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-115-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PEPPER TREE POLLEN 
    schinus molle injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-412
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SCHINUS MOLLE POLLEN (UNII: M0G28FH9K1) (SCHINUS MOLLE POLLEN - UNII:M0G28FH9K1) SCHINUS MOLLE POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-412-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-412-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-412-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-412-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PHOMA 
    phoma betae injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-116
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLEOSPORA BETAE (UNII: V58BK047ES) (PLEOSPORA BETAE - UNII:V58BK047ES) PLEOSPORA BETAE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-116-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-116-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-116-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-116-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    POVERTY WEED POLLEN 
    iva axillaris injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-363
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IVA AXILLARIS POLLEN (UNII: 13KFG30UBR) (IVA AXILLARIS POLLEN - UNII:13KFG30UBR) IVA AXILLARIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-363-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-363-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-363-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-363-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PRIVET POLLEN 
    ligustrum vulgare injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-376
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E) LIGUSTRUM VULGARE POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-376-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-376-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-376-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-376-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PULLULARIA 
    pullularia pullulans injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-117
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-117-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-117-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-117-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-117-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    PUSSY WILLOW POLLEN 
    salix discolor injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-407
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALIX DISCOLOR POLLEN (UNII: ER172J09FM) (SALIX DISCOLOR POLLEN - UNII:ER172J09FM) SALIX DISCOLOR POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-407-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-407-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-407-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-407-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    QUACKGRASS POLLEN 
    agropyron repens injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-307
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (ELYMUS REPENS POLLEN - UNII:ON2T85TA2O) ELYMUS REPENS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-307-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-307-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-307-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-307-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RABBITBUSH POLLEN 
    ambrosia deltoides injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-354
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP) (AMBROSIA DELTOIDEA POLLEN - UNII:O4AB4546TP) AMBROSIA DELTOIDEA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-354-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-354-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-354-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-354-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RED ALDER POLLEN 
    alnus rubra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-435
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (ALNUS RUBRA POLLEN - UNII:Z0F2YK1B7H) ALNUS RUBRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-435-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-435-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-435-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-435-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RED CEDAR POLLEN 
    juniperus virginiana injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-373
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-373-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-373-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-373-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-373-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RED MAPLE POLLEN 
    acer rubrum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-434
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-434-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-434-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-434-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-434-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RED MULBERRY POLLEN 
    morus rubra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-447
    Route of AdministrationSUBCUTANEOUS, INTRADERMAL, CUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-447-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-447-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-447-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-447-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RED OAK POLLEN 
    quercus rubra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-450
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-450-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-450-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-450-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-450-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    REDROOT PIGWEED POLLEN 
    amaranthus retroflexus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-314
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-314-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-314-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-314-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-314-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RHIZOPUS 
    rhizopus oryzae injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-118
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-118-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-118-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-118-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-118-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RIVER/RED BIRCH POLLEN 
    betula nigra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-443
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-443-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-443-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-443-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-443-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ROCKY MTN. JUNIPER POLLEN 
    juniperus scopulorum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-372
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (JUNIPERUS SCOPULORUM POLLEN - UNII:0G82TT8ZFY) JUNIPERUS SCOPULORUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-372-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-372-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-372-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-372-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ROUGH MARSHELDER POLLEN 
    iva ciliata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-364
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-364-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-364-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-364-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-364-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RUSSIAN OLIVE POLLEN 
    elaeagnus angustifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-346
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ELAEAGNUS ANGUSTIFOLIA POLLEN (UNII: 68P4F4M6VD) (ELAEAGNUS ANGUSTIFOLIA POLLEN - UNII:68P4F4M6VD) ELAEAGNUS ANGUSTIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-346-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-346-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-346-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-346-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RUSSIAN THISTLE POLLEN 
    salsola kali injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-410
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G) SALSOLA KALI POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-410-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-410-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-410-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-410-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    RUST, WHEAT 
    puccinia striiformis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-120
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PUCCINIA STRIIFORMIS VAR. STRIIFORMIS (UNII: 9NLW29GJAX) (PUCCINIA STRIIFORMIS VAR. STRIIFORMIS - UNII:9NLW29GJAX) PUCCINIA STRIIFORMIS VAR. STRIIFORMIS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-120-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-120-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-120-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-120-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SALT CEDAR POLLEN 
    tamarix gallica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-415
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TAMARIX GALLICA POLLEN (UNII: 43IR7KR479) (TAMARIX GALLICA POLLEN - UNII:43IR7KR479) TAMARIX GALLICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-415-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-415-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-415-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-415-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SALT GRASS POLLEN 
    distichlis spicata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-345
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DISTICHLIS SPICATA POLLEN (UNII: GOA51670YV) (DISTICHLIS SPICATA POLLEN - UNII:GOA51670YV) DISTICHLIS SPICATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-345-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-345-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-345-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-345-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SANDBUR RAGWEED POLLEN 
    ambrosia bipinnatifida injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-353
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA CHAMISSONIS POLLEN (UNII: 2Z41EEQ491) (AMBROSIA CHAMISSONIS POLLEN - UNII:2Z41EEQ491) AMBROSIA CHAMISSONIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-353-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-353-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-353-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-353-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SHAD SCALE POLLEN 
    atriplex confertifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-439
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATRIPLEX CONFERTIFOLIA POLLEN (UNII: GG8WX068MX) (ATRIPLEX CONFERTIFOLIA POLLEN - UNII:GG8WX068MX) ATRIPLEX CONFERTIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-439-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-439-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-439-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-439-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SHAGBARK HICKORY POLLEN 
    carya ovata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-332
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-332-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-332-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-332-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-332-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SHEEP SORREL POLLEN 
    rumex acetosella injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-405
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-405-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-405-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-405-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-405-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SHORTLEAF PINE POLLEN 
    pinus echinata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-448
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PINUS ECHINATA POLLEN (UNII: 96LRW14765) (PINUS ECHINATA POLLEN - UNII:96LRW14765) PINUS ECHINATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-448-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-448-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-448-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-448-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SILVER MAPLE POLLEN 
    acer saccharinum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-304
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER SACCHARINUM POLLEN (UNII: 95447163DG) (ACER SACCHARINUM POLLEN - UNII:95447163DG) ACER SACCHARINUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-304-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-304-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-304-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-304-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SILVER RAGWEED POLLEN 
    dicoria canescens injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-344
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DICORIA CANESCENS POLLEN (UNII: E9H4GR1NMP) (DICORIA CANESCENS POLLEN - UNII:E9H4GR1NMP) DICORIA CANESCENS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-344-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-344-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-344-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-344-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SISAL 
    sisal injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-021
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AGAVE SISALANA FIBER (UNII: MRJ91HVV4H) (AGAVE SISALANA FIBER - UNII:MRJ91HVV4H) AGAVE SISALANA FIBER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-021-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-021-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-021-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-021-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SLENDER RAGWEED POLLEN 
    ambrosia tenuifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-356
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA TENUIFOLIA POLLEN (UNII: 57W5SO585B) (AMBROSIA TENUIFOLIA POLLEN - UNII:57W5SO585B) AMBROSIA TENUIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-356-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-356-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-356-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-356-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SMOOTH BROME POLLEN 
    bromus inermis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-328
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (BROMUS INERMIS POLLEN - UNII:766QT72BK6) BROMUS INERMIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-328-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-328-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-328-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-328-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SMUT, CORN 
    ustilago maydis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-122
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-122-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-122-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-122-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-122-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SMUT, JOHNSON GRASS 
    sphacelotheca cruenta injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-123
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SPORISORIUM CRUENTUM (UNII: GQM6LVU5V8) (SPORISORIUM CRUENTUM - UNII:GQM6LVU5V8) SPORISORIUM CRUENTUM0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-123-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-123-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-123-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-123-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SMUT, WHEAT 
    tilletia caries (tritici) injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-124
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TILLETIA CARIES (UNII: C7000B9PQI) (TILLETIA CARIES - UNII:C7000B9PQI) TILLETIA CARIES0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-124-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-124-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-124-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-124-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SPRING BIRCH POLLEN 
    betula fontinalis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-441
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976) (BETULA OCCIDENTALIS POLLEN - UNII:R889N2L976) BETULA OCCIDENTALIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-441-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-441-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-441-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-441-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    STEMPHYLIUM 
    stemphylium botryosum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-126
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLEOSPORA TARDA (UNII: TPL549N9R8) (PLEOSPORA TARDA - UNII:TPL549N9R8) PLEOSPORA TARDA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-126-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-126-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-126-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-126-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SUGAR BEET POLLEN 
    beta vulgaris injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-324
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETA VULGARIS POLLEN (UNII: W7NU4B5CIY) (BETA VULGARIS POLLEN - UNII:W7NU4B5CIY) BETA VULGARIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-324-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-324-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-324-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-324-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SUNFLOWER POLLEN 
    helianthus annua injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-360
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HELIANTHUS ANNUUS POLLEN (UNII: 28D6K7E9IP) (HELIANTHUS ANNUUS POLLEN - UNII:28D6K7E9IP) HELIANTHUS ANNUUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-360-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-360-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-360-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-360-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    SWEET GUM POLLEN 
    liquidamber styraciflua injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-377
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS) LIQUIDAMBAR STYRACIFLUA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-377-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-377-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-377-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-377-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    TAG ALDER POLLEN 
    alnus rugosa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-436
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-436-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-436-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-436-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-436-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    TOBACCO LEAF 
    tobacco leaf injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-022
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-022-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-022-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-022-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-022-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    TREE OF HEAVEN POLLEN 
    ailanthus altissima injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-310
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (AILANTHUS ALTISSIMA POLLEN - UNII:2A64U81OQ3) AILANTHUS ALTISSIMA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-310-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-310-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-310-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-310-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    UTAH JUNIPER POLLEN 
    juniperus osteosperma injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-370
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS OSTEOSPERMA POLLEN (UNII: 15L060HV8H) (JUNIPERUS OSTEOSPERMA POLLEN - UNII:15L060HV8H) JUNIPERUS OSTEOSPERMA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-370-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-370-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-370-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-370-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    VELVET GRASS POLLEN 
    holcus lanatus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-361
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (HOLCUS LANATUS POLLEN - UNII:70O1TP6H01) HOLCUS LANATUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-361-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-361-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-361-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-361-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WESTERN JUNIPER POLLEN 
    juniperus occidentalis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-369
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS OCCIDENTALIS POLLEN (UNII: 7JWJ3HXZ9U) (JUNIPERUS OCCIDENTALIS POLLEN - UNII:7JWJ3HXZ9U) JUNIPERUS OCCIDENTALIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-369-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-369-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-369-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-369-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WESTERN RAGWEED POLLEN 
    ambrosia psilostachia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-316
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-316-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-316-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-316-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-316-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WESTERN SYCAMORE POLLEN 
    platanus racemosa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-392
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLATANUS RACEMOSA POLLEN (UNII: BWC8DYU8OS) (PLATANUS RACEMOSA POLLEN - UNII:BWC8DYU8OS) PLATANUS RACEMOSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-392-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-392-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-392-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-392-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WESTERN WATERHEMP POLLEN 
    acnida tamariscina injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-305
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (AMARANTHUS TUBERCULATUS POLLEN - UNII:92N6W6KO2G) AMARANTHUS TUBERCULATUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-305-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-305-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-305-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-305-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WESTERN WHEATGRASS POLLEN 
    agropyron smithii injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-308
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O) (PASCOPYRUM SMITHII POLLEN - UNII:6AU0ZD8T1O) PASCOPYRUM SMITHII POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-308-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-308-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-308-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-308-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WHITE ASH POLLEN 
    fraxinus americana injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-357
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-357-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-357-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-357-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-357-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WHITE HICKORY POLLEN 
    carya tomentosa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-334
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ALBA POLLEN (UNII: G2A764T54B) (CARYA ALBA POLLEN - UNII:G2A764T54B) CARYA ALBA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-334-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-334-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-334-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-334-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WHITE MULBERY POLLEN 
    morus alba injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-382
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-382-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-382-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-382-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-382-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WHITE OAK POLLEN 
    quercus alba injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-402
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-402-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-402-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-402-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-402-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WHITE POPLAR POLLEN 
    populus alba injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-394
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P) POPULUS ALBA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-394-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-394-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-394-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-394-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WING SCALE POLLEN 
    atriplex canescens injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-438
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (ATRIPLEX CANESCENS POLLEN - UNII:26U0BU8G83) ATRIPLEX CANESCENS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-438-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-438-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-438-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-438-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WINTERFAT POLLEN 
    eurotia lanata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-348
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KRASCHENINNIKOVIA LANATA POLLEN (UNII: 0GTO5BR99M) (KRASCHENINNIKOVIA LANATA POLLEN - UNII:0GTO5BR99M) KRASCHENINNIKOVIA LANATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-348-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-348-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-348-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-348-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WORMWOOD SAGE POLLEN 
    artemisia absinthium injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-319
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA ABSINTHIUM POLLEN (UNII: 81GS97HVFO) (ARTEMISIA ABSINTHIUM POLLEN - UNII:81GS97HVFO) ARTEMISIA ABSINTHIUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-319-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-319-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-319-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-319-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    YELLOW PINE POLLEN 
    pinus ponderosa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-449
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PINUS PONDEROSA POLLEN (UNII: 042SUA2DS9) (PINUS PONDEROSA POLLEN - UNII:042SUA2DS9) PINUS PONDEROSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-449-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-449-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-449-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-449-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ACACIA POLLEN 
    acacia spp. injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-301
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACACIA POLLEN (UNII: 43DDR2YDYZ) (ACACIA POLLEN - UNII:43DDR2YDYZ) ACACIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-301-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-301-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-301-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-301-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    WALNUT MIX 
    walnut mix injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-544
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.0167 g  in 1 mL
    JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1) JUGLANS REGIA POLLEN0.0167 g  in 1 mL
    JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I) (JUGLANS CALIFORNICA POLLEN - UNII:2147EPR64I) JUGLANS CALIFORNICA POLLEN0.0167 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 g  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-544-011 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:49643-544-055 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:49643-544-1010 mL in 1 VIAL; Type 0: Not a Combination Product
    4NDC:49643-544-3030 mL in 1 VIAL; Type 0: Not a Combination Product
    5NDC:49643-544-5050 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ALTERNARIA 
    alternaria alternata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-101
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    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
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-101-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-101-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-101-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-101-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ALDER, WHITE POLLEN 
    alnus rhombifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-312
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (ALNUS RHOMBIFOLIA POLLEN - UNII:7X8HL8GRTM) ALNUS RHOMBIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-312-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-312-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-312-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-312-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ALFALFA POLLEN 
    medicago sativa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-300
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY) MEDICAGO SATIVA POLLEN0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-300-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-300-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-300-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-300-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ALKALI BLITE POLLEN 
    suaeda spp. injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-414
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SUAEDA NIGRA POLLEN (UNII: FZU040QDS7) (SUAEDA NIGRA POLLEN - UNII:FZU040QDS7) SUAEDA NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-414-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-414-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-414-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-414-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    AMERICAN ELM POLLEN 
    ulmus americana injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-417
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-417-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-417-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-417-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-417-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ARIZONA ASH POLLEN 
    fraxinus velutina injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-359
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD) FRAXINUS VELUTINA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-359-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-359-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-359-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-359-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ARROYO WILLOW POLLEN 
    salix lasiolepsis injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-408
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALIX LASIOLEPIS POLLEN (UNII: 808UWJ59FI) (SALIX LASIOLEPIS POLLEN - UNII:808UWJ59FI) SALIX LASIOLEPIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-408-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-408-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-408-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-408-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ASPEN POLLEN 
    populus tremuloides injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-398
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (POPULUS TREMULOIDES POLLEN - UNII:928OC2TJDA) POPULUS TREMULOIDES POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-398-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-398-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-398-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-398-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-130
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-130-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-130-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-130-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-130-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    AUSTRALIAN PINE POLLEN 
    casuarina equisetifoli injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-335
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (CASUARINA EQUISETIFOLIA POLLEN - UNII:OZJ4OE173N) CASUARINA EQUISETIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-335-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-335-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-335-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-335-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BAHIA GRASS POLLEN 
    paspalum notatum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-384
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-384-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-384-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-384-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-384-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BASSIA POLLEN 
    bassia hyssopifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-323
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BASSIA HYSSOPIFOLIA POLLEN (UNII: 35487N1IC9) (BASSIA HYSSOPIFOLIA POLLEN - UNII:35487N1IC9) BASSIA HYSSOPIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-323-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-323-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-323-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-323-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BEECH POLLEN 
    fagus grandifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-349
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-349-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-349-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-349-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-349-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BLACK COTTONWOOD POLLEN 
    populus trichocarpa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-399
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS TRICHOCARPA POLLEN (UNII: H8QYU50Z2D) (POPULUS TRICHOCARPA POLLEN - UNII:H8QYU50Z2D) POPULUS TRICHOCARPA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-399-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-399-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-399-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-399-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BLACK OAK POLLEN 
    quercus velutina injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-451
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS VELUTINA POLLEN (UNII: 294L626TT0) (QUERCUS VELUTINA POLLEN - UNII:294L626TT0) QUERCUS VELUTINA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-451-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-451-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-451-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-451-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BLACK WALNUT POLLEN 
    juglans nigra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-366
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-366-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-366-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-366-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-366-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BLACK WILLOW POLLEN 
    salix nigra injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-409
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-409-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-409-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-409-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-409-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BOTRYTIS 
    botrytis cinerea injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-104
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    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
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-104-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-104-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-104-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-104-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BOTTLEBRUSH POLLEN 
    callistemon citrinus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-330
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALLISTEMON CITRINUS POLLEN (UNII: 62OII98F1T) (CALLISTEMON CITRINUS POLLEN - UNII:62OII98F1T) CALLISTEMON CITRINUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-330-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-330-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-330-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-330-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BOX ELDER MAPLE POLLEN 
    acer negundo injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-303
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-303-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-303-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-303-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-303-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BURNING BUSH POLLEN 
    kochia scoparia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-374
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5) BASSIA SCOPARIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-374-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-374-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-374-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-374-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BURROBRUSH POLLEN 
    hymenoclea salsola injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-362
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA SALSOLA POLLEN (UNII: 662J7FTA7T) (AMBROSIA SALSOLA POLLEN - UNII:662J7FTA7T) AMBROSIA SALSOLA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-362-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-362-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-362-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-362-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    BURWEED MARSHELDER POLLEN 
    iva xanthifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-365
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-365-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-365-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-365-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-365-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CALIF. BLACK WALNUT POLLEN 
    juglans californica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-446
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I) (JUGLANS CALIFORNICA POLLEN - UNII:2147EPR64I) JUGLANS CALIFORNICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-446-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-446-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-446-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-446-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CALIFORNIA JUNIPER POLLEN 
    juniperus californica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-368
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L) JUNIPERUS CALIFORNICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-368-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-368-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-368-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-368-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CALIFORNIA SCRUB OAK POLLEN 
    quercus dumosa injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-403
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS DUMOSA POLLEN (UNII: P5W45RU6E4) (QUERCUS DUMOSA POLLEN - UNII:P5W45RU6E4) QUERCUS DUMOSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-403-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-403-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-403-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-403-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CANARY GRASS POLLEN 
    phalaris arundinaceae injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-385
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9) (PHALARIS ARUNDINACEA POLLEN - UNII:FAY1Y90VJ9) PHALARIS ARUNDINACEA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-385-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-385-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-385-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-385-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CANDIDA 
    candida albicans injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-105
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-105-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-105-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-105-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-105-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CANYON RAGWEED POLLEN 
    ambrosia ambrosioides injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-352
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA AMBROSIOIDES POLLEN (UNII: 81214Y871U) (AMBROSIA AMBROSIOIDES POLLEN - UNII:81214Y871U) AMBROSIA AMBROSIOIDES POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-352-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-352-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-352-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-352-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CARELESS WEED POLLEN 
    amaranthus palmerii injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-313
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH) AMARANTHUS PALMERI POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-313-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-313-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-313-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-313-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CATTLE EPITHELIA 
    cattle epithelia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-003
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-003-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-003-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-003-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-003-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CEPHALOSPORIUM 
    cephalosporium roseum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-106
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CEPHALOSPORIUM ROSEUM (UNII: 1756J4PM8P) (CEPHALOSPORIUM ROSEUM - UNII:1756J4PM8P) CEPHALOSPORIUM ROSEUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-106-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-106-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-106-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-106-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CHAETOMIUM 
    chaetomium globosum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-107
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-107-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-107-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-107-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-107-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CHEAT GRASS POLLEN 
    bromus secalinus injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-329
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046) (BROMUS SECALINUS POLLEN - UNII:Q4T1SJ3046) BROMUS SECALINUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-329-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-329-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-329-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-329-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CHERRY BIRCH POLLEN 
    betula lenta injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-442
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-442-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-442-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-442-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-442-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CHINESE ELM POLLEN 
    ulmus pumila injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-419
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ULMUS PUMILA POLLEN (UNII: 030R993R8E) (ULMUS PUMILA POLLEN - UNII:030R993R8E) ULMUS PUMILA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-419-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-419-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-419-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-419-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CLADOSPORIUM 
    cladosporium herbarum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-108
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    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
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-108-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-108-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-108-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-108-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COAST LIVE OAK POLLEN 
    quercus agrifolia injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-401
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7) QUERCUS AGRIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-401-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-401-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-401-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-401-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COAST MAPLE POLLEN 
    acer macrophyllum injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-302
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER MACROPHYLLUM POLLEN (UNII: E4CG5Q55M1) (ACER MACROPHYLLUM POLLEN - UNII:E4CG5Q55M1) ACER MACROPHYLLUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-302-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-302-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-302-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-302-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COAST SAGE POLLEN 
    artemisia californica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-437
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA CALIFORNICA POLLEN (UNII: 1EDY616508) (ARTEMISIA CALIFORNICA POLLEN - UNII:1EDY616508) ARTEMISIA CALIFORNICA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-437-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-437-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-437-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-437-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COCKLEBUR POLLEN 
    xanthium commune injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-420
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-420-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-420-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-420-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-420-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COCKROACH, AMERICAN 
    periplaneta americana injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-047
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-047-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-047-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-047-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-047-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COCKROACH, GERMAN 
    blattella germanica injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-048
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-048-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-048-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-048-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-048-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COMMON SAGE POLLEN 
    artemisia tridentata injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-320
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD) ARTEMISIA TRIDENTATA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-320-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-320-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-320-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-320-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    CORN POLLEN POLLEN 
    zea mays injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-422
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZEA MAYS POLLEN (UNII: 74PD8J616H) (ZEA MAYS POLLEN - UNII:74PD8J616H) ZEA MAYS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-422-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-422-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-422-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-422-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    COTTON LINTERS 
    cotton linters injection
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:49643-004
    Route of AdministrationINTRADERMAL, CUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO) COTTON FIBER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.0025 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00125 g  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.53 g  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 g  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49643-004-055 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2NDC:49643-004-1010 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3NDC:49643-004-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    4NDC:49643-004-5050 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10221103/12/1974
    Labeler - Allermed Laboratories, Inc. (073364531)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allermed Laboratories, Inc.073364531manufacture