Label: ANIMAL ALLERGENS, AP CATTLE HAIR AND DANDER- cattle hair and dander injection, solution
ANIMAL ALLERGENS, AP DOG HAIR AND DANDER CANIS SPP- animal allergens, dog dander canis spp injection, solution
ANIMAL ALLERGENS, DOG HAIR AND DANDER CANIS SPP.- dog hair canis spp. injection, solution
ANIMAL ALLERGENS, AP HORSE HAIR AND DANDER- ap horse hair .......ction, solution
POLLENS - TREES, MULBERRY MIX- mulberry mix injection, solution
POLLENS - TREES, OAK MIX- oak mix injection, solution
POLLENS - TREES, OAK, RED QUERCUS RUBRA- oak, red quercus rubra injection, solution
ANIMAL ALLERGENS, UF DOG HAIR-DANDER CANIS SPP- animal allergens, dog dander canis spp injection, solution

  • NDC Code(s): 65044-0854-2, 65044-0854-3, 65044-0854-4, 65044-0856-2, view more
    65044-0856-3, 65044-0856-4, 65044-0879-4, 65044-1006-2, 65044-1006-3, 65044-1006-4, 65044-1018-2, 65044-1018-3, 65044-1018-4, 65044-1021-2, 65044-1021-3, 65044-1021-4, 65044-1060-2, 65044-1060-3, 65044-1060-4, 65044-1081-2, 65044-1081-3, 65044-1081-4, 65044-1084-2, 65044-1084-3, 65044-1084-4, 65044-1120-2, 65044-1120-3, 65044-1120-4, 65044-1168-2, 65044-1168-3, 65044-1168-4, 65044-1171-2, 65044-1171-3, 65044-1171-4, 65044-1172-2, 65044-1172-3, 65044-1172-4, 65044-1207-2, 65044-1207-3, 65044-1207-4, 65044-1213-2, 65044-1213-3, 65044-1213-4, 65044-1216-2, 65044-1216-3, 65044-1216-4, 65044-1217-2, 65044-1217-3, 65044-1217-4, 65044-1237-2, 65044-1237-3, 65044-1237-4, 65044-1297-2, 65044-1297-3, 65044-1297-4, 65044-1300-2, 65044-1300-3, 65044-1300-4, 65044-1303-2, 65044-1303-3, 65044-1303-4, 65044-1336-2, 65044-1336-3, 65044-1336-4, 65044-1339-2, 65044-1339-3, 65044-1339-4, 65044-1342-2, 65044-1342-3, 65044-1342-4, 65044-1343-2, 65044-1343-3, 65044-1343-4, 65044-1405-2, 65044-1405-3, 65044-1405-4, 65044-1408-2, 65044-1408-3, 65044-1408-4, 65044-1409-2, 65044-1409-3, 65044-1409-4, 65044-1414-2, 65044-1414-3, 65044-1414-4, 65044-1435-2, 65044-1435-3, 65044-1435-4, 65044-1438-2, 65044-1438-3, 65044-1438-4, 65044-1450-2, 65044-1450-3, 65044-1450-4, 65044-1453-2, 65044-1453-3, 65044-1453-4, 65044-1516-2, 65044-1516-3, 65044-1516-4, 65044-1519-2, 65044-1519-3, 65044-1519-4, 65044-1520-2, 65044-1520-3, 65044-1520-4, 65044-1540-2, 65044-1540-3, 65044-1540-4, 65044-1543-2, 65044-1543-3, 65044-1543-4, 65044-1544-2, 65044-1544-3, 65044-1544-4, 65044-1546-2, 65044-1546-3, 65044-1546-4, 65044-1564-2, 65044-1564-3, 65044-1564-4, 65044-1630-2, 65044-1630-3, 65044-1630-4, 65044-1660-2, 65044-1660-3, 65044-1660-4, 65044-1662-2, 65044-1662-3, 65044-1662-4, 65044-1663-2, 65044-1663-3, 65044-1663-4, 65044-1702-2, 65044-1702-3, 65044-1702-4, 65044-1744-2, 65044-1744-3, 65044-1744-4, 65044-1747-2, 65044-1747-3, 65044-1747-4, 65044-1780-2, 65044-1780-3, 65044-1780-5, 65044-1783-2, 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65044-2074-2, 65044-2074-3, 65044-2074-4, 65044-2098-2, 65044-2098-3, 65044-2098-4, 65044-2101-2, 65044-2101-3, 65044-2101-4, 65044-2107-2, 65044-2107-3, 65044-2107-4, 65044-2125-2, 65044-2125-3, 65044-2125-4, 65044-2203-2, 65044-2203-3, 65044-2203-4, 65044-2212-2, 65044-2212-3, 65044-2212-4, 65044-2215-2, 65044-2215-3, 65044-2215-4, 65044-2216-2, 65044-2216-3, 65044-2216-4, 65044-2217-2, 65044-2217-3, 65044-2217-4, 65044-2251-2, 65044-2251-3, 65044-2251-4, 65044-2293-2, 65044-2293-3, 65044-2293-4, 65044-2296-2, 65044-2296-3, 65044-2296-4, 65044-2308-2, 65044-2308-3, 65044-2308-4, 65044-2311-2, 65044-2311-3, 65044-2311-4, 65044-2320-2, 65044-2320-3, 65044-2320-4, 65044-2359-2, 65044-2359-3, 65044-2359-4, 65044-2362-2, 65044-2362-3, 65044-2362-4, 65044-2413-2, 65044-2413-3, 65044-2413-4, 65044-2416-2, 65044-2416-3, 65044-2416-4, 65044-2417-2, 65044-2417-3, 65044-2417-4, 65044-2482-2, 65044-2482-3, 65044-2482-4, 65044-2485-2, 65044-2485-3, 65044-2485-4, 65044-2487-2, 65044-2487-3, 65044-2487-4, 65044-2506-2, 65044-2506-3, 65044-2506-4, 65044-2508-2, 65044-2508-3, 65044-2508-4, 65044-2563-2, 65044-2563-3, 65044-2563-4, 65044-2599-2, 65044-2599-3, 65044-2599-4, 65044-2619-2, 65044-2619-3, 65044-2619-4, 65044-2622-2, 65044-2622-3, 65044-2622-4, 65044-2623-2, 65044-2623-3, 65044-2623-4, 65044-2624-2, 65044-2624-3, 65044-2624-4, 65044-2626-2, 65044-2626-3, 65044-2626-4, 65044-2629-2, 65044-2629-3, 65044-2629-4, 65044-2632-2, 65044-2632-3, 65044-2632-4, 65044-2633-2, 65044-2633-3, 65044-2633-4, 65044-2634-2, 65044-2634-3, 65044-2634-4, 65044-2635-2, 65044-2635-3, 65044-2635-4, 65044-2677-2, 65044-2677-3, 65044-2677-4, 65044-2854-2, 65044-2854-3, 65044-2854-4, 65044-2855-2, 65044-2855-3, 65044-2855-4, 65044-2856-2, 65044-2856-3, 65044-2856-4, 65044-2861-2, 65044-2861-3, 65044-2861-4, 65044-2862-2, 65044-2862-3, 65044-2862-4, 65044-2863-2, 65044-2863-3, 65044-2863-4, 65044-3014-2, 65044-3020-2, 65044-3041-2, 65044-3074-2, 65044-3077-2, 65044-3107-2, 65044-3116-2, 65044-3125-2, 65044-3134-2, 65044-3140-2, 65044-3173-2, 65044-3191-2, 65044-3203-2, 65044-3212-2, 65044-3215-2, 65044-3248-2, 65044-3254-2, 65044-3305-2, 65044-3362-2, 65044-3380-2, 65044-3389-2, 65044-3428-2, 65044-3449-2, 65044-3452-2, 65044-3455-2, 65044-3461-2, 65044-3509-2, 65044-3518-2, 65044-3548-2, 65044-3554-2, 65044-3565-2, 65044-3584-2, 65044-3596-2, 65044-3626-2, 65044-3656-2, 65044-3674-2, 65044-3695-2, 65044-3713-2, 65044-3716-2, 65044-4083-2, 65044-4083-3, 65044-4083-4, 65044-4085-2, 65044-4085-3, 65044-4085-4, 65044-4349-2, 65044-4349-3, 65044-4349-4, 65044-4352-2, 65044-4352-3, 65044-4352-4, 65044-4401-2, 65044-4811-2, 65044-4811-3, 65044-4811-4, 65044-4824-2, 65044-4824-3, 65044-4824-4, 65044-4850-2, 65044-4850-4, 65044-4855-2, 65044-4855-3, 65044-4855-4, 65044-5000-2, 65044-5000-3, 65044-5000-4, 65044-5004-2, 65044-5004-3, 65044-5004-4, 65044-5008-2, 65044-5008-3, 65044-5008-4, 65044-5020-2, 65044-5020-3, 65044-5020-4, 65044-5032-2, 65044-5032-3, 65044-5032-4, 65044-5048-2, 65044-5048-3, 65044-5048-4, 65044-5052-1, 65044-5052-3, 65044-5052-4, 65044-5055-1, 65044-5055-3, 65044-5055-4, 65044-5056-2, 65044-5056-3, 65044-5056-4, 65044-5076-2, 65044-5076-3, 65044-5076-4, 65044-5100-2, 65044-5100-3, 65044-5100-4, 65044-5104-2, 65044-5104-3, 65044-5104-4, 65044-5112-2, 65044-5112-3, 65044-5112-4, 65044-5124-2, 65044-5124-3, 65044-5124-4, 65044-5128-2, 65044-5128-3, 65044-5128-4, 65044-5136-2, 65044-5136-3, 65044-5136-4, 65044-5144-2, 65044-5144-3, 65044-5144-4, 65044-5168-2, 65044-5168-3, 65044-5168-4, 65044-5208-2, 65044-5208-3, 65044-5208-4, 65044-5220-2, 65044-5220-3, 65044-5220-4, 65044-5230-2, 65044-5230-3, 65044-5230-4, 65044-5235-2, 65044-5235-3, 65044-5235-4, 65044-5264-2, 65044-5264-3, 65044-5264-4, 65044-5284-2, 65044-5284-3, 65044-5284-4, 65044-6513-2, 65044-6517-2, 65044-6517-3, 65044-6517-4, 65044-6518-2, 65044-6518-3, 65044-6518-4, 65044-6580-2, 65044-6580-3, 65044-6580-4, 65044-6581-2, 65044-6581-3, 65044-6581-4, 65044-6584-2, 65044-6584-3, 65044-6584-4, 65044-6587-2, 65044-6587-3, 65044-6587-4, 65044-6588-2, 65044-6588-3, 65044-6588-4, 65044-6589-2, 65044-6589-3, 65044-6589-4, 65044-6590-2, 65044-6590-3, 65044-6590-4
  • Packager: Jubilant HollisterStier LLC
  • Category: NON-STANDARDIZED ALLERGENIC LABEL
  • DEA Schedule: None
  • Marketing Status: Biologic Licensing Application

Drug Label Information

Updated November 1, 2023

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

  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use NON‑STANDARDIZED ALLERGENIC EXTRACTS (POLLENS, MOLDS, EPIDERMALS AND INSECTS) safely and effectively.  See full prescribing information for NON-STANDARDIZED ALLERGENIC EXTRACTS (POLLENS, MOLDS, EPIDERMALS AND INSECTS).

    NON-STANDARDIZED ALLERGENIC EXTRACTS (POLLENS, MOLDS, EPIDERMALS AND INSECTS)

    Solution for percutaneous, intradermal, or subcutaneous administration Initial U.S. Approval:  1925

    WARNING:  ANAPHYLAXIS

    See full prescribing information for complete boxed warning.

    • Non-standardized allergenic extracts can cause anaphylaxis, including anaphylactic shock and death.(5.1)
    • Do not administer to individuals with severe, unstable or uncontrolled asthma, history of severe systemic reaction to the allergen extract when administered for diagnosis or treatment, or with medical conditions that reduce the ability to survive anaphylaxis.(4)
    • Observe individuals for at least 30 minutes following administration.Emergency measures and personnel trained in their use must be available in the event of a life-threatening reaction.(5.1)
    • Individuals with extreme sensitivity to these products, on an accelerated immunotherapy build-up, switching to another lot, receiving high doses of these products, or exposed to similar allergens may be at increased risk of anaphylaxis.(5.1)
    • These products may not be suitable for individuals who may be unresponsive to epinephrine or inhaled bronchodilators, such as those taking beta-blockers.(5.1)

    INDICATIONS AND USAGE

    Non-standardized allergenic extracts are indicated for:

    • Skin test diagnosis of patients with a clinical history of allergy to the specific corresponding allergens.(1)
    • Immunotherapy for the reduction of allergen-induced allergic symptoms confirmed by positive skin test or by in vitro testing for allergen-specific IgE antibodies.(1)

    DOSAGE AND ADMINISTRATION

    For percutaneous, intradermal, or subcutaneous use only.

    Administration:

    • Percutaneous for diagnostic testing.
    • Intradermal for diagnostic testing.
    • Subcutaneous for immunotherapy.

    See full prescribing information for details on dosing and dilution preparation.  (2)

    DOSAGE FORMS AND STRENGTHS

    Non-standardized allergenic extract solutions:  stock concentrates, labeled in weight/volume, in a glycerin-preserved extracting fluid, supplied in 5, 10, 30, and 50 mL vials.  (3, 16)  Refer to the vial label for the product concentration.  (11)

    CONTRAINDICATIONS

    • Severe, unstable or uncontrolled asthma.(4)
    • History of any severe systemic reaction to the allergen extract when administered for diagnosis or treatment.(4)
    • Medical conditions that reduce the ability to survive anaphylaxis.(4)

    WARNINGS AND PRECAUTIONS

    The risk of anaphylaxis may be increased in the following situations:

    • Extreme sensitivity to non-standardized allergenic extracts.
    • Concomitant environmental exposure to similar allergens.
    • Receipt of high concentrations and volumes of non-standardized allergenic extracts.
    • Receipt of an accelerated build-up schedule (e.g., "rush" immunotherapy).
    • Changing to another lot of allergen.(5)

    ADVERSE REACTIONS

    Common adverse reactions reported for non-standardized allergenic extracts are:

    • Local adverse reactions, occurring in 26 to 82% of all patients who receive subcutaneous immunotherapy (e.g., erythema, swelling, pruritus, tenderness and pain at the injection site).(6)
    • Systemic adverse reactions, occurring in ≤ 7% of patients who receive subcutaneous immunotherapy (e.g., generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, and hypotension).Systemic reactions may be fatal.(6)

    To report SUSPECTED ADVERSE REACTIONS, contact Jubilant HollisterStier at 1-800-495-7437 or Adverse.Reactions@jhs.jubl.com; or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    DRUG INTERACTIONS

    • Certain medications may decrease skin test wheal and erythema responses, including antihistamines, topical corticosteroids, topical anesthetics, and tricyclic antidepressants.(7)

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 11/2023

  • Table of Contents
  • BOXED WARNING (What is this?)

    WARNING:  ANAPHYLAXIS

    • Non-standardized allergenic extracts can cause anaphylaxis, including anaphylactic shock and death.(5.1)
    • Do not administer to individuals with:
      • severe, unstable or uncontrolled asthma;
      • history of severe systemic reaction to the allergen extract when administered for diagnosis of treatment;
      • medical conditions that reduce the ability to survive anaphylaxis.(4)
    • Observe individuals for at least 30 minutes following administration. Emergency measures and personnel trained in their use must be available in the event of a life-threatening reaction.(5.1)
    • Individuals with extreme sensitivity to these products, on an accelerated immunotherapy build-up, switching to another lot, receiving high doses of these products, or exposed to similar allergens may be at increased risk of anaphylaxis.(5.1)
    • These products may not be suitable for individuals who may be unresponsive to epinephrine or inhaled bronchodilators, such as those taking beta-blockers.(5.1)

  • 1 INDICATIONS AND USAGE

    NON-STANDARDIZED ALLERGENIC EXTRACTS are indicated for:

    • Skin test diagnosis of individuals with a clinical history of allergy to the specific corresponding allergens.

    NON-STANDARDIZED ALLERGENIC EXTRACTS are indicated for:

    • Immunotherapy for the reduction of allergen-induced allergic symptoms confirmed by positive skin test or by in vitro testing for allergen specific IgE antibodies for the specific corresponding allergens.
  • 2 DOSAGE AND ADMINISTRATION

    For percutaneous, intradermal, or subcutaneous administration only.  Do not inject intravenously.

    2.1 Preparation for Administration

    Appearance is clear to slightly opalescent.  Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.  Discard solution if either of these conditions exist.

    Non-standardized allergenic extracts diluted with Albumin Saline with Phenol (0.4%) (stabilized diluent) may be more potent than extracts diluted with diluents that do not contain albumin.  When switching from non-stabilized to stabilized diluent, consider less concentrated initial dilutions for both intradermal testing and immunotherapy.

    Different formulations, preparations, or new lots of non-standardized allergenic extracts are not interchangeable.  Dosing should be adjusted appropriately when formulations, preparations, or lots of non-standardized allergenic extracts are changed [see Immunotherapy (2.3) and Dosage Forms and Strengths (3)].

    Allergenic extracts may be prepared for intradermal (diagnosis) or subcutaneous (immunotherapy) administration by diluting stock concentrates.

    • For diluent, use sterile albumin saline with phenol or sterile normal saline with phenol.
    • Dilute stock concentrates by a minimum of 100-fold for intradermal testing.  Dilutions of 1,000-fold or greater are appropriate starting points for patients with a clinical history of adverse reaction.

    To prepare dilutions for intradermal testing and immunotherapy, start with a stock concentrate, and prepare a ten-fold (1:10) dilution by adding 0.5 mL of concentrate to 4.5 mL of sterile aqueous diluent.  Prepare subsequent dilutions in a similar manner.  (see Table 1).

    Table 1:  10-fold Dilution Series

    Dilution

    Extract

    Milliliters of Diluent

    Dilution Strength (w/v)

    Dilution Strength (w/v)

    Dilution Strength (w/v)

    Dilution Strength (w/v)

    Dilution Strength (w/v)

    0

    Concentrate

    1:10

    1:20

    1:50

    1:100

    1:650

    1

    0.5 mL Concentrate

    4.5

    1:100

    1:200

    1:500

    1:1,000

    1:6,500

    2

    0.5 mL Dilution

    4.5

    1:1,000

    1:2,000

    1:5,000

    1:10,000

    1:65,000

    3

    0.5 mL Dilution 2

    4.5

    1:10,000

    1:20,000

    1:50,000

    1:100,000

    1:650,000

    4

    0.5 mL Dilution 3

    4.5

    1:100,000

    1:200,000

    1:500,000

    1:1,000,000

    1:6,500,000

    5

    0.5 mL Dilution 4

    4.5

    1:1,000,000

    1:2,000,000

    1:5,000,000

    1:10,000,000

    1:65,000,000

    6

    0.5 mL Dilution 5

    4.5

    1:10,000,000

    1:20,000,000

    1:50,000,000

    1:100,000,000

    1:650,000,000

    Note: A lower starting dose and/or less concentrated dilutions may be necessary for highly sensitive patients with a clinical history of sensitivity, or for those who display severe symptoms. [see Diagnostic Testing (2.2),Percutaneous Skin Testing (2.2.1) and Intradermal (Intracutaneous) Skin Test (2.2.2)].

    2.2 Diagnostic Testing

    Testing is performed to identify patients that exhibit an allergic response at the site of administration.  False positive reactions may occur.  A positive skin test reaction must be interpreted in the context of the individual’s clinical history and known exposure to the allergen.

    • Administer percutaneous tests prior to administration of intradermal tests to identify highly sensitive patients.
    • Do not use allergen mixes for diagnostic testing because a positive reaction would not permit specific identification of the allergen(s) that elicited the reaction.  In addition, a negative reaction would fail to indicate whether an individual component allergen would have elicited a positive reaction at full strength.

    2.2.1 Percutaneous Skin Testing

    Dose

    Unless an individual is suspected to be at greater risk for anaphylaxis, the initial starting dose is 1 drop (approximately 0.05 mL) of undiluted allergenic extract.  For individuals suspected to be at greater risk for anaphylaxis (for example, as indicated by a history of allergen-induced anaphylaxis), initiate percutaneous testing with a sequence of serial 10-fold dilutions of undiluted allergenic extract spaced 15‑20 minutes apart [see Preparation for Administration (2.1)].

    Administration

    • Percutaneous Test:  Place one drop (approximately 0.05 mL) of allergen on the skin and pierce through drop superficially into the skin, lifting slightly.  Use a skin test device, such as a sterile needle, lancet, or bifurcated needle.
    • Percutaneous Test using self-loading devices:  Refer to the manufacturer’s product instructions.

    Concurrently, use a positive histamine skin test control to identify patients whose recent use of drugs with antihistamine activity may result in a false negative skin test.  Apply a 50% glycerin solution as a negative control, to identify false positive responses to the extracting fluid used in the manufacture of allergenic extracts, or due to dermographism [see Drug Interactions (7)].

     

    Interpreting Results

    For interpretation of percutaneous skin tests, refer to the information provided in Allergy Diagnostic Testing:  An Updated Practice Parameter.1  In addition, follow the directions provided with the percutaneous skin test devices.  Measure wheal responses for the histamine positive control test at 15 minutes and for the allergen tests at 15 to 20 minutes.

    • The negative control (50% glycerin solution) response should measure < 3 mm wheal and ≤ 10 mm flare.1
    • Response to positive controls should be at least 3 millimeters larger than the response to the negative control.
    • If either the response to the histamine positive control or to the negative control do not meet the criteria above for acceptable wheal size, the results for the allergenic extracts tested at the same time should be considered invalid and be repeated.
    • Fire Ant:  Percutaneous testing is considered positive when the response occurs at a concentration of 1:100 w/v or less.4

    2.2.2 Intradermal (Intracutaneous) Skin Test

    Always perform percutaneous tests prior to intradermal skin tests.1, 2

    Dose

    Perform intradermal tests with at least 100-fold less concentrated solutions than the stock concentrates used in percutaneous tests [see Preparation and Administration (2.1)].

    Fire Ant:  Use 0.02 mL of a 1:100,000 v/v dilution of the concentrate for intradermal tests.  Very sensitive individuals such as those who have had nearly fatal anaphylactic reactions may not tolerate even 1:100,000 v/v dilution of concentrate as a starting point.  These patients should be tested with a 1:10,000,000 v/v dilution of concentrate [see Preparation for Administration (2.1)].

    Use intradermal tests following a negative or equivocal percutaneous test when the patient continues to report a history of symptoms following exposure to a specific allergen.

    Administration

    Intradermally inject 0.02 mL of the allergen using a 1 mL intradermal testing syringe with a 26 or 27 gauge, 1/2" or 3/8" needle with intradermal bevel, graduated in 0.01 units.  Insert needle at a 30˚ angle, bevel down.

    Test concurrently with a positive histamine control at intradermal strength (0.1 mg/mL of histamine base) and an aqueous buffer negative control (Sterile Albumin Saline with Phenol, Sterile Buffered Saline with Phenol).

    Interpreting Results

    For interpretation of intradermal skin tests, follow the information provided in Allergy Diagnostic Testing:  An Updated Practice Parameter.1

    • Measure wheal responses for the histamine positive control test and allergen tests at 10‑15 minutes after injection
    • Response to the positive control should be at least 3 millimeters larger than the response to the negative control.
    • The negative control (50% glycerin solution) response should measure < 3‑mm wheal and ≤ 10 mm flare (erythema).
    • If either the response to the histamine positive control or to the negative control do not meet the criteria above for acceptable wheal size, the results for the allergenic extracts tested at the same time should be considered invalid and be repeated.
    • Fire Ant:  Intradermal testing is considered positive when the response occurs at a concentration of 1:1,000 w/v or less.4

    2.3 Immunotherapy

    For subcutaneous administration only.

     

    Administration of Immunotherapy

    Administer immunotherapy by subcutaneous injection in the lateral aspect of the arm or thigh.  Avoid injection directly into any blood vessels.  Administer injections with a sterile 1 mL allergy treatment syringe with a 26 or 27 gauge, 1/2", beveled needle, graduated in 0.01 units.

    The optimal interval between doses of allergenic extract varies among individuals.  Injections are usually given one or two times per week until the maintenance dose is reached, at which time the injection interval is increased to 2, 3, and finally 4 weeks.

    Most adverse reactions occur within 30 minutes after injection.  Therefore, observe patients for at least 30 minutes.  For high risk patients, 30 minutes of observation may not be sufficient.2

    Dosing of non-standardized allergenic extracts for allergen immunotherapy is highly individualized.  Adjust dose according to the degree of sensitivity of the patient, tolerance to the extract administered during the early phases of an injection regimen, and the clinical response.  Dosing is individualized by choice of an initial dose, the schedule of dose build-up, the target maintenance dose, the actual maintenance dose, and the duration of treatment.

    The large volume of solution for immunotherapy may produce increased discomfort in the pediatric population.  In order to achieve the total dose required, the volume of the dose may need to be divided into more than one injection per visit.²

    2.3.1 Dose Build-up

    Following the first administration of 0.03 mL of the selected initial dilution of allergenic extract, dosing is increased in 0.03 mL to 0.12 mL increments until 0.3 mL is reached, following which 0.03 mL is administered from the next most concentrated allergen extract or allergen mixture vial in the dilution series.  The interval between doses is usually 3 to 7 days during dose build-up.  Proceed in this manner until a maintenance dose is reached.  The final maintenance dose may not be the target maintenance dose selected at the beginning of therapy.

    The following adjustments may be necessary during dose build-up:

    • If allergic symptoms or local reactions develop shortly after dose administration, decrease the dose volume to one-half or one-quarter of the maximum dose previously attained.
    • If the patient is experiencing any seasonal allergy symptoms, decrease the dose volume to one-half or one‑quarter of the maximum dose previously attained.
    • Adjust the dose periodically based on the patient’s tolerance and reaction.
    • Decrease the dose if the previous injection resulted in a marked local reaction.
    • Repeat the previous dose or reduce the dose at the next administration if local reactions persist for longer than 24 hours.
    • Decrease the dose if the previous injection resulted in a systemic reaction.Any evidence of a systemic reaction is an indication for a significant (at least 75%) reduction in the subsequent dose or the cessation of immunotherapy.
    • Repeated systemic reactions, however mild, are sufficient reason for the cessation of further attempts to increase the reaction-causing dose.

    2.3.2 Maintenance Dose Selection, Adjustments, and Intervals

    The maintenance dose is the dose that provides therapeutic efficacy without severe adverse local or systemic reactions.  This dose may be limited by adverse reactions and may not be the original targeted maintenance dose.  Select a maintenance dose based on the patient's clinical response and tolerance.

    • Suggested maintenance dose is 0.3 mL of the undiluted allergen extract.  Occasionally, higher doses are necessary to relieve symptoms.
    • Maintenance doses larger than 0.3 mL of undiluted allergen extract may cause patient discomfort due to the 50% glycerin content.
    • After the maintenance dose is achieved, increase the injection interval to 2 weeks, then 3 weeks, and finally 4 weeks, as tolerated.  Administer the maintenance dose at a given interval three or four times before further increasing the interval to assure that no reactions occur.  Protection may be lost rapidly if the interval between doses is more than 4 weeks.

    The following adjustments to the maintenance dose may be necessary.

     

     Withhold immunotherapy and/or reduce dosage, if any of the following conditions exist:

    • Severe symptoms of rhinitis and/or asthma.  Decrease dose to one-half or one-quarter of the maximum dose previously attained if the patient has any seasonal symptoms.
    • Allergic symptoms or a local reaction following the prior dose.
    • Infection accompanied by fever.
    • Exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection.

    In situations prompting dose reduction, a cautious increase in dosage can be attempted once the reduced dose is tolerated.

    Decrease the interval between doses if symptoms develop before the next injection is scheduled.

    In some patients, the dosage may be increased and/or the dosing interval shortened based on individual responses and dosing requirements.  If the onset of symptoms is soon after the initiation of immunotherapy, decrease the interval between each dose.

    Changing to a different lot of extract:  All extracts can lose allergenic activity over time and extracts vary in allergenic activity.  Two different lots of extract could differ substantially in allergenic activity, even if they are the same formula and concentration.  The volume of the first dose from the new vial should not exceed 50% of the previous dose.  Do not use extracts beyond their expiry date.

    Changing to a different formulation of extract or to an extract from a different manufacturer:  Decrease the starting dose of the new extract when the extract is the same formula and dilution as the one previously used.  In general, a volume dose reduction to 50% of the previous product dose is adequate, but each situation must be evaluated separately considering the patient's history of sensitivity, tolerance of previous injections, and other factors.  If the patient tolerates the 50% decrease, then raise the next dose to the previous tolerated dose amount.  To re-establish the maintenance dose the starting interval between doses should not be greater than one week.

    Prolonged period has elapsed since the last injection:  Patients may lose tolerance for allergen injections during prolonged intervals (> 4 weeks) between doses.  The duration of tolerance is an individual characteristic and varies from patient to patient.  In general, the longer the lapse in the injection schedule, the greater dose reduction required.

    Changes made in the extract concentrate formula:  Changes other than those listed above such as a difference in extracting fluid (e.g., change from non-glycerin extracts to 50% glycerin extracts), combining two or more stock concentrates, or any other change can affect a patient’s tolerance of the treatment.  Extra dilutions are recommended whenever starting a revised formula.  The greater the change, the greater the number of dilutions required.

    Duration of Treatment

    The duration of treatment for immunotherapy has not been established.  A period of two to three years of injection therapy constitutes an average minimum course of treatment.  Evaluate patients for treatment response at least every 6 to 12 months while they receive immunotherapy.

  • 3 DOSAGE FORMS AND STRENGTHS

    Non-standardized allergenic extracts are solutions: stock concentrates, labeled in weight/volume, in a glycerin-preserved extracting fluid, supplied in 5, 10, 30, and 50 mL vials.  (3, 16)  Refer to the vial label for the product concentration.  (11)

  • 4 CONTRAINDICATIONS

    Non-standardized allergenic extracts are contraindicated in individuals with the following conditions:

    • Severe, unstable or uncontrolled asthma.
    • History of any severe systemic reaction to the allergen extract when administered for diagnosis or treatment.
    • Medical conditions that reduce the ability to survive anaphylaxis.
  • 5 WARNINGS AND PRECAUTIONS

    5.1 Anaphylaxis

    Anaphylaxis, which may lead to death, can occur in individuals following the administration of non-standardized allergenic extracts, particularly in the following situations:

    • Extreme sensitivity to the non-standardized allergenic extract.
    • Concomitant environmental exposure to allergens.
    • Receipt of high doses of the non-standardized allergenic extract.
    • Receipt of an accelerated build-up schedule (“rush” immunotherapy).
    • Change from one lot of a particular non-standardized allergenic extract to another lot of the same non-standardized allergenic extract.

    Administer non-standardized allergenic extracts in a healthcare setting under the supervision of a physician prepared to manage anaphylaxis; management may include use of inhaled bronchodilators and use of epinephrine.  Non-standardized allergenic extracts may not be suitable for individuals who may be unresponsive to epinephrine or inhaled bronchodilators, such as those taking beta-blockers.  See prescribing information for epinephrine for complete information, particularly on medications that blunt or potentiate epinephrine activity.  Individuals should remain in the physician’s office for a minimum of 30 minutes after receiving an injection of non‑standardized allergenic extracts, so that any adverse reaction can be observed and properly handled.

    5.2 Cross-reactions and Dose Sensitivity

    When determining the final dose of an allergen mixture for immunotherapy, consider cross-reactivity among component extracts.

    Determine the initial dilution of allergenic extract, starting dose, and progression of dosage based on the patient’s history and results of skin tests [see Dosage and Administration (2)].  Strongly positive skin tests can be indicators for potential adverse reactions.

  • 6 ADVERSE REACTIONS

    Common adverse reactions reported for non-standardized allergenic extracts are:

    • Local reactions occurring in 26 to 82% of all patients who receive subcutaneous immunotherapy, at the injection site (e.g., erythema, swelling, pruritus, tenderness and pain).2
    • Systemic adverse reactions, occurring in ≤ 7% of patients who receive subcutaneous immunotherapy (e.g., generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, hypotension, and shock).3  Systemic reactions may be fatal.2

     

    No clinical trials of non-standardized allergenic extracts have been conducted.

    Published studies of non-standardized allergenic extracts report systemic reactions occurring in fewer than 1% in patients receiving conventional immunotherapy and greater than 36% in patients receiving rush immunotherapy.  Most systemic reactions occurred within 30 minutes of injection.  However, systemic reactions have been reported to occur up to 2 hours after the final injection with rush schedules.  Some reactions have occurred up to 6 hours after skin tests or immunotherapy.2, 3

  • 7 DRUG INTERACTIONS

    7.1 Antihistamines

    Do not perform skin testing with non-standardized allergenic extracts within 3 to 10 days of first-generation H1-histamine receptor blockers (e.g., clemastine, diphenhydramine) and second-generation antihistamines (e.g., loratadine, fexofenadine) being used.  These products suppress histamine skin test reactions and could mask a positive response.1, 2

    7.2 Topical Corticosteroids and Topical Anesthetics

    Topical corticosteroids may suppress skin reactivity; therefore, discontinue use at the skin test site for at least 2 to 3 weeks before skin testing.  Avoid use of topical local anesthetics at skin test sites because they can suppress flare responses.1, 2

    7.3 Tricyclic Antidepressants

    Tricyclic antidepressants, such as doxepin, can have potent antihistamine effects and may alter skin test results.  Allow 7 to 14 days after discontinuation of tricyclic medication prior to skin testing.1, 2

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    All pregnancies have a risk of birth defect, loss, or other adverse outcomes.  In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.  There are no human or animal data to establish the presence or absence of non-standardized allergenic extracts‑associated risks during pregnancy.

    8.2 Lactation

    Risk Summary

    It is not known whether non-standardized allergenic extracts are present in human milk.  Data are not available to assess the effects of these extracts on the breastfed child or on milk production/excretion.  The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for non-standardized allergenic extracts and any potential adverse effects on the breastfed child from the extracts or from the underlying maternal condition.

    8.4 Pediatric Use

    For use of these products in children younger than 5 years of age, consideration should be given to the patient’s ability to comply and cooperate with receipt of the product and the potential for difficulty in communicating with the child regarding systemic reactions.²

    The volume of a dose for immunotherapy may need to be divided for pediatric patients [see Dosage and Administration (2.3)]

    8.5 Geriatric Use

    Data are not available to determine if subjects 65 years of age and older respond differently to allergen immunotherapy than younger subjects.

  • 11 DESCRIPTION

    Non-standardized allergenic extracts are labeled “No U.S.  Standard of Potency”.

    Non-standardized allergenic extracts are supplied in a Glycero Cocas extraction solution, which consists of 0.5% sodium chloride for isotonicity, 0.275% sodium bicarbonate as a buffer, and 50% glycerin (volume/volume) as preservative.

    Non-standardized allergenic extracts are supplied as a weight to volume (w/v) solution of allergen in extraction solution.  Product concentrations vary based on the source.  Refer to the vial label for the product concentration.

    Source material mold mycelia and Candida albicans cells are cultivated on liquid medium which may contain one or more of the following constituents:  casein hydrolysate; malt extract; yeast extract; maltose; dextrose; ammonium nitrate, calcium carbonate, calcium chloride, ammonium citrate, potassium phosphate, sodium citrate, citric acid; magnesium sulfate; or trace elements.  Acetone and ether may be used as drying and de-fatting agents.  Candida albicans cells are treated with phenol, which is removed by dialysis.

    Dog Hair and Dander extracts are manufactured in 3 product forms:

    • Dog Hair and Dander (Regular Process) is derived from extraction of the source material without additional processing, and is prepared at 1:10 w/v in Glycero-Cocas.
    • Acetone Precipitated (AP) Dog Hair and Dander is derived from the acetone precipitated aqueous extract and is prepared at 1:100 w/v in Glycero-Cocas.
    • Ultrafiltered (UF) Dog Hair and Dander is derived from the UF aqueous extract and is prepared at 1:650 w/v in Glycero‑Cocas.
  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    The skin test reaction results from interaction of the introduced allergen and allergen-specific IgE antibodies bound to mast cells, leading to mast cell degranulation and release of histamine, tryptase and other mediators, which results in the formation of the wheal and flare.

    The precise mechanisms of action of allergen immunotherapy are not known.  Immunologic responses to immunotherapy include changes in allergen-specific IgE levels, allergen-specific IgG levels, and regulatory T cell responses.2

  • 14 CLINICAL STUDIES

    Specific immunotherapy with allergenic extracts is helpful in reducing symptoms associated with exposure to the offending allergens.  A summary of effectiveness by the Panel on Review of Allergenic Extracts, an advisory committee to the U.S.  Food and Drug Administration, has been published.5

  • 15 REFERENCES

    1.  Bernstein IL, Li JT, Bernstein Dl, et al.  Allergy diagnostic testing:  and updated practice parameter.  Ann Allergy Asthma Immunol.  2008 Mar;100:S1-148.

    2.  Cox L, Nelson H, Lockey R, Calabria C, Chacko T, Finegold I, et al.  Allergen immunotherapy:  A practice parameter third update.  J Allergy Clin Immunol.  2011 Jan;127:S1-55.

    3.  Greineder DK.  Risk management in allergen immunotherapy.  J Allergy Clin Immunol.  1996 Dec;98(6 Pt 3):S330-4

    4.  Golden D B K, Demain J, Freeman T, Graft D, et al.  Stinging insect hypersensitivity:  A practice parameter update 2016.  Ann Allergy Asthma Immunol 118 (2017) 28-54.

    5.  Federal Register Proposed Rule:  Biological Products:  Implementation of Efficacy Review, Allergenic Extracts, Federal Register 1985;50:3082-3288.

  • 16 HOW SUPPLIED

    Non-standardized allergenic extracts and mixes are supplied as 50% glycerin stock concentrates labeled in weight/volume and provided in 10 milliliter, 30 milliliter and 50 milliliter vials for use in percutaneous skin testing and subcutaneous immunotherapy.  These extracts may also be supplied in 5 milliliter dropper vials for percutaneous testing only.

    These products are supplied as listed in Table 2.

    TABLE 2: AVAILABLE PRODUCTS

    POLLEN – GRASS ALLERGENS

    Bahia Grass,Paspalum notatum

    Brome, SmoothBromus inermis

    Corn, CultivatedZea mays

    Grass Mix 8-100,000 BAU/mL each ofP. pratensis; A. gigantean; P. pretense;10,000 BAU/mL ofC. dactylon; 1:20w/v ofS. halepense

    Johnson Grass,Sorghum halepense

    Oats, Common Cultivated,Avena sativa

    POLLEN – TREE ALLERGENS

    Acacia, Golden,Acacia longifolia

    Alder, Red,Alnus rubra

    Ash, White,Fraxinus americana

    Beech, American,Fagus grandifolia

    Birch Mix (PRW)-B. papyrifera, B. pendula, B. nigra

    Bottlebrush,Melaleuca citrina

    Boxelder/Maple Mix (BHR)-A. negundo, A. saccharum, A. rubrum

    Cedar, Mountain,Juniperus ashei

    Cedar, Red,Juniperus virginiana

    Cottonwood, Common,Populus deltoides

    Cyprus, Arizona,Cupressus arizonica

    Cyprus, Bald,Taxodium distichum

    Elm, American,Ulmus americana

    Elm, Chinese,Ulmus parvifolia

    Gum, Sweet,Liquidambar styraciflua

    Hackberry,Celtis occidentalis

    Hickory, Shagbark,Carya ovata

    Maple, Hard/Sugar,Acer saccharum

    Melaleuca,Melaleuca quinquenervia

    Mesquite,Prosopis glandulosa

    Mulberry Mix (RW)-M. rubra, M. alba

    Oak Mix (RVW)-Q. rubra, Q. virginiana, Q. alba

    Oak, Red,Quercus Rubra

    Olive Tree,Olea europaea

    Palm, Queen,Syagrus romanzoffiana

    Pecan Tree,Carya illinoinensis

    Pine Mix (LY)-P. contorta, P. ponderosa

    Privet, Common,Ligustrum vilgare

    Russian Olive,Elaeagnus angustifolia

    Sycamore, American,Platanus occidentalis

    Tree Mix 5-20% each ofF. Americana; J. nigra; P. deltoides; U. Americana;6.7% each ofB. papyrifera; B. nigra; B. pendula

    Tree Mix 6- Tree Mix 6-20% each ofF. Americana; J. nigra; P. deltoides; U. Americana;6.7% each ofB. papyrifera; B. nigra; B. pendula

    Tree Mix 11-10% each ofF. americana; B. nigra; J. nigra; P. deltoides; U. americana; C. ovata; A. saccharum; Q. rubra; P. occidentalis; S. nigra

    Walnut, Black,Juglans nigra

    Willow, Black,Salix nigra

    POLLEN – WEED AND GARDEN PLANT ALLERGENS

    Careless Weed,Amaranthus palmeri

    Careless/Pigweed Mix (CR)-A. palmeri, A. retroflexus

    Cocklebur, Common,Xanthium strumarium

    Dock/Sorrel Mix (DS)-R. crispus, R. acetosella

    Dog Fennel, Eastern,Eupatorium capillifolium

    Goldenrod,Solidago canadensis

    Kochia,Kochia scoparia

    Lamb’s Quarters,Chenopodium album

    Marshelder/Poverty Mix (BPT)-C. xanthifolia, I. annua, I. axillaris

    Nettle,Urtica dioica

    Pigweed, Rough Redroot,Amaranthus retroflexus

    Plantain, English,Plantago lanceolata

    Ragweed, Giant,Ambrosia trifida

    Ragweed Mix (GSW)-A. trifida, A. artemisiifolia, A. psilostachya

    Ragweed, Western,Ambrosia psilostachya

    Russian Thistle,Salcola kali

    Sagebrush, Mugwort,Artemisia vulgaris

    Scale, Wing,Atriplex canescens

    Sorrel, Sheep,Rumex acetosella

    Weed Mix 2630-25% each ofX. strumarium; C. album; A. retroflexus;12.5% each ofR. crispus; R. acetosella

    MOLDS

    Alternaria/Hormodendrum Mix-A. tenuis, H. cladosporioides

    Alternaria tenuis (Alternariaalternata)

    Aspergillus fumigatus

    Aspergillus niger var. niger

    Botrytis cinerea

    Candida albicans

    Cephalosporium acremonium (Sarocladiumstrictum)

    Curvularia spicifera (Cochliobolusspicifer)

    Epicoccum nigrum

    Epidermophyton floccosum

    Fusarium vasinfectum (Fusariumoxysporumvasinfectum)

    Heliminthosporium interseminatum (Dendryphiellavinosa)

    Hormodendrum cladosporioides (Cladosporium cladosporioides)

    Mold Mix 4-25% each ofA. alternata; C. cladosporioides;6.2% each ofA. fumigatus; A. nidulans; A. nigervar. niger; A. terreus; P. digitatum; P. expansum; P. chrysogenumvar. chrysogenum; C. rosea f. rosea

    Mold Mix 10-2.5% each ofA. fumigatus; A. nidulans; A. nigervar. niger; A. terreus; P. digitatum; P. expansum; P. chrysogenumvar. chrysogenum; C. roseaf. rosea;10% each ofA. alternata; F. oxysporumvasinfectum; D. vinosa; C. cladosporioides; M. racemosus; P. exiguavar. exigua; A. pullulansvar. pullutans; R. stolonifer

    Mucor racemosus

    Penicillium Mix-P. expansum, P. digitatum, P. chrysogenum, C. rosea

    Penicillium notatum (Penicilliumchrysogenumvar. chrysogenum)

    Phoma herbarum (Phomaexiguavar. exigua)

    Pullularia pullulans (Aerobasidiumpullulansvar. pullulans)

    Rhizopus nigricans (Rhizopusstolonifer)

    Stemphylium botryosum (Pleosporatarda)

    Trichophyton Mix-T. tonsurans, T. rubrum , T. mentagrophytes

    EPIDERMALS

    AP Horse Hair and Dander,Equuscaballus

    AP Cattle Hair and Dander,Bostaurus

    AP Dog Hair and Dander,Canislupusfamiliaris

    Dog Hair and Dander,Canislupusfamiliaris

    UF Dog Hair and Dander,Canislupusfamiliaris

    Feather Mix-G. gallus,A. platyrhynchos, A. anser

    Guinea Pig Hair and Dander,Caviaporcellus

    INSECTS

    Cockroach, American,Periplanetaamericana

    Cockroach, German,Blatellagermanica

    Cockroach Mix-P. americana, B. germanica

    Fire Ant,Solenopsisinvicta


    16.2 Storage and Handling

    Store extracts at 2°C to 8°C (36°F to 46°F).

  • 17 PATIENT COUNSELING INFORMATION

    Instruct patients to remain in the office under observation for a minimum of 30 minutes after an injection or longer, if deemed necessary for the individual.

    Inform patients that reactions may occur more than 30 minutes after skin testing or an injection.

    Instruct patient to recognize the following symptoms as systemic adverse reactions and seek emergency medical care right away if any of these symptoms occur:

    • Unusual swelling and/or tenderness at the injection site.
    • Hives or itching of the skin.
    • Swelling of face and/or mouth.
    • Sneezing, coughing, or wheezing.
    • Shortness of breath.
    • Nausea.
    • Dizziness or faintness.

    Manufacturer:

    Jubilant HollisterStier LLC

    Spokane, WA 99207 U.S.A.

    U.S. Lic. No. 1272

    Version Date: February 24, 2022

  • PRINCIPAL DISPLAY PANEL

    UF Dog Hair-Dander, 10 mL 1.650wv Carton Label

    UF Dog Hair-Dander, 10 mL 1.650wv Carton Label

    UF Dog Hair-Dander, 10 mL 1.650wv Vial Label

    UF Dog Hair-Dander, 10 mL 1.650wv Vial Label

  • INGREDIENTS AND APPEARANCE
    ANIMAL ALLERGENS, AP CATTLE HAIR AND DANDER 
    cattle hair and dander injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4811
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS HAIR (UNII: TOQ97Z8644) (BOS TAURUS HAIR - UNII:TOQ97Z8644) BOS TAURUS HAIR0.01 g  in 1 mL
    BOS TAURUS DANDER (UNII: C8VYS726O8) (BOS TAURUS DANDER - UNII:C8VYS726O8) BOS TAURUS DANDER0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4811-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4811-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4811-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388801/30/1978
    ANIMAL ALLERGENS, AP DOG HAIR AND DANDER CANIS SPP 
    animal allergens, dog dander canis spp injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4824
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (CANIS LUPUS FAMILIARIS HAIR - UNII:05S7L91ZTR) CANIS LUPUS FAMILIARIS HAIR0.005 g  in 1 mL
    CANIS LUPUS FAMILIARIS DANDER (UNII: 11JCK302I4) (CANIS LUPUS FAMILIARIS DANDER - UNII:11JCK302I4) CANIS LUPUS FAMILIARIS DANDER0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4824-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4824-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4824-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388808/24/1976
    ANIMAL ALLERGENS, DOG HAIR AND DANDER CANIS SPP. 
    dog hair canis spp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4083
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (CANIS LUPUS FAMILIARIS HAIR - UNII:05S7L91ZTR) CANIS LUPUS FAMILIARIS HAIR0.05 g  in 1 mL
    CANIS LUPUS FAMILIARIS DANDER (UNII: 11JCK302I4) (CANIS LUPUS FAMILIARIS DANDER - UNII:11JCK302I4) CANIS LUPUS FAMILIARIS DANDER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4083-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4083-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4083-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    ANIMAL ALLERGENS, DOG HAIR AND DANDER CANIS SPP. 
    dog hair canis spp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4085
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (CANIS LUPUS FAMILIARIS HAIR - UNII:05S7L91ZTR) CANIS LUPUS FAMILIARIS HAIR0.05 g  in 1 mL
    CANIS LUPUS FAMILIARIS DANDER (UNII: 11JCK302I4) (CANIS LUPUS FAMILIARIS DANDER - UNII:11JCK302I4) CANIS LUPUS FAMILIARIS DANDER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4085-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4085-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4085-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    ANIMAL ALLERGENS, AP HORSE HAIR AND DANDER 
    ap horse hair and dander injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4855
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUUS CABALLUS HAIR (UNII: 4F35XG0149) (EQUUS CABALLUS HAIR - UNII:4F35XG0149) EQUUS CABALLUS HAIR0.01 g  in 1 mL
    EQUUS CABALLUS DANDER (UNII: J81SZ18495) (EQUUS CABALLUS DANDER - UNII:J81SZ18495) EQUUS CABALLUS DANDER0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4855-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4855-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4855-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388801/30/1978
    ANIMAL ALLERGENS, FEATHER MIX 
    feather mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4349
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (GALLUS GALLUS FEATHER - UNII:1FCM16V0FV) GALLUS GALLUS FEATHER0.1 g  in 1 mL
    ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (ANAS PLATYRHYNCHOS FEATHER - UNII:83B65P4796) ANAS PLATYRHYNCHOS FEATHER0.1 g  in 1 mL
    ANSER ANSER FEATHER (UNII: 15XI414745) (ANSER ANSER FEATHER - UNII:15XI414745) ANSER ANSER FEATHER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4349-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4349-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4349-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    ANIMAL ALLERGENS, FEATHER MIX 
    feather mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4352
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (GALLUS GALLUS FEATHER - UNII:1FCM16V0FV) GALLUS GALLUS FEATHER0.1 g  in 1 mL
    ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (ANAS PLATYRHYNCHOS FEATHER - UNII:83B65P4796) ANAS PLATYRHYNCHOS FEATHER0.1 g  in 1 mL
    ANSER ANSER FEATHER (UNII: 15XI414745) (ANSER ANSER FEATHER - UNII:15XI414745) ANSER ANSER FEATHER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4352-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-4352-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-4352-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    ANIMAL ALLERGENS, GUINEA PIG HAIR AND DANDER 
    guinea pig hair and dander injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4401
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAVIA PORCELLUS HAIR (UNII: KBA5Y6X57N) (CAVIA PORCELLUS HAIR - UNII:KBA5Y6X57N) CAVIA PORCELLUS HAIR0.05 g  in 1 mL
    CAVIA PORCELLUS DANDER (UNII: 84Q71TU5SU) (CAVIA PORCELLUS DANDER - UNII:84Q71TU5SU) CAVIA PORCELLUS DANDER0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-4401-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - ANIMAL PRODUCTS AND POULTRY PRODUCTS, BEEF BOVINE SPP. 
    beef bovine spp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3077
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BEEF (UNII: 4PIB2155QP) (BEEF - UNII:4PIB2155QP) BEEF0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3077-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - ANIMAL PRODUCTS AND POULTRY PRODUCTS, CHICKEN MEAT GALLUS SP. 
    chicken meat gallus sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3173
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POULTRY, UNSPECIFIED (UNII: L7WXO2P5HM) (POULTRY, UNSPECIFIED - UNII:L7WXO2P5HM) POULTRY, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3173-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, OLIVE OLEA EUROPAEA 
    olive olea europaea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2053
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2053-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2053-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2053-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PALM, QUEEN COCOS PLUMOSA 
    palm, queen cocos plumosa injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2074
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB) SYAGRUS ROMANZOFFIANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2074-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2074-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2074-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PALO VERDE CERCIDIUM FLORIDUM 
    palo verde cercidium floridum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2018
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2018-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2018-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2018-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PECAN CARYA CARYA ILLINOENSIS 
    pecan carya carya illinoensis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2098
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2098-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2098-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2098-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PECAN CARYA CARYA ILLINOENSIS 
    pecan carya carya illinoensis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2101
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2101-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2101-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2101-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PEPPER TREE, CALIFORNIA SCHINUS MOLLE 
    pepper tree, california schinus molle injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2107
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2107-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2107-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2107-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PINE MIX 
    pine mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2203
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PINUS CONTORTA POLLEN (UNII: FB7IP650ET) (PINUS CONTORTA POLLEN - UNII:FB7IP650ET) PINUS CONTORTA POLLEN0.05 g  in 1 mL
    PINUS PONDEROSA POLLEN (UNII: 042SUA2DS9) (PINUS PONDEROSA POLLEN - UNII:042SUA2DS9) PINUS PONDEROSA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2203-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2203-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2203-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, PRIVET LIGUSTRUM VULGARE 
    privet ligustrum vulgare injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2251
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2251-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2251-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2251-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, RUSSIAN OLIVE ELAEAGNUS ANGUSTIFOLIA 
    russian olive elaeagnus angustifolia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2359
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2359-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2359-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2359-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, SYCAMORE, AMERICAN EASTERN PLATANUS OCCIDENTALLIS 
    sycamore, american eastern platanus occidentallis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2563
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2563-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2563-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2563-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 11 
    tree mix 11 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2619
    Route of AdministrationPERCUTANEOUS, 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
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.05 g  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.05 g  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN0.05 g  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN0.05 g  in 1 mL
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN0.05 g  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.05 g  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN0.05 g  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN0.05 g  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2619-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2619-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2619-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 11 
    tree mix 11 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2622
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN0.1 g  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.1 g  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.1 g  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN0.1 g  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN0.1 g  in 1 mL
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN0.1 g  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.1 g  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN0.1 g  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN0.1 g  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2622-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2622-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2622-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 11 
    tree mix 11 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2624
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN20000 [PNU]  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN20000 [PNU]  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN20000 [PNU]  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN20000 [PNU]  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN20000 [PNU]  in 1 mL
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN20000 [PNU]  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN20000 [PNU]  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN20000 [PNU]  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN20000 [PNU]  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2624-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2624-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2624-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 11 
    tree mix 11 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2623
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN40000 [PNU]  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN40000 [PNU]  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN40000 [PNU]  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN40000 [PNU]  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN40000 [PNU]  in 1 mL
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN40000 [PNU]  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN40000 [PNU]  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN40000 [PNU]  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN40000 [PNU]  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2623-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2623-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2623-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 5 
    tree mix 5 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2854
    Route of AdministrationPERCUTANEOUS, 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
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.017 g  in 1 mL
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN0.017 g  in 1 mL
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN0.017 g  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN0.017 g  in 1 mL
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN0.017 g  in 1 mL
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN0.017 g  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN0.05 g  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2854-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2854-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2854-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 5 
    tree mix 5 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2856
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN0.1 g  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.033 g  in 1 mL
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN0.033 g  in 1 mL
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN0.033 g  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN0.033 g  in 1 mL
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN0.033 g  in 1 mL
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN0.033 g  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN0.1 g  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2856-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2856-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2856-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 5 
    tree mix 5 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2855
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN20000 [PNU]  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN20000 [PNU]  in 1 mL
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN20000 [PNU]  in 1 mL
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN20000 [PNU]  in 1 mL
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN20000 [PNU]  in 1 mL
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN20000 [PNU]  in 1 mL
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN20000 [PNU]  in 1 mL
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN20000 [PNU]  in 1 mL
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA POLLEN - UNII:6M2JIH93ZN) SALIX NIGRA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2855-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2855-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2855-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 6 
    tree mix 6 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2863
    Route of AdministrationPERCUTANEOUS, 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
    BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN0.017 g  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.017 g  in 1 mL
    BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN0.017 g  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.05 g  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN0.05 g  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2863-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2863-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2863-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 6 
    tree mix 6 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2861
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN0.1 g  in 1 mL
    BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN0.033 g  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.033 g  in 1 mL
    BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN0.033 g  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.1 g  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN0.1 g  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2861-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2861-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2861-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE MIX 6 
    tree mix 6 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2862
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN20000 [PNU]  in 1 mL
    BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN20000 [PNU]  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN20000 [PNU]  in 1 mL
    BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN20000 [PNU]  in 1 mL
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN20000 [PNU]  in 1 mL
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN20000 [PNU]  in 1 mL
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2862-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2862-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2862-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, TREE OF HEAVEN AILANTHUS ALTISSIMA 
    tree of heaven ailanthus altissima injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2599
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2599-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2599-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2599-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, WALNUT, BLACK JUGLANS NIGRA 
    walnut, black juglans nigra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2626
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2626-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2626-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2626-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, WALNUT, BLACK JUGLANS NIGRA 
    walnut, black juglans nigra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2629
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2629-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2629-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2629-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, WILLOW, BLACK SALIX NIGRA 
    willow, black salix nigra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2677
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2677-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2677-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2677-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, COCKLEBUR XANTHIUM STRUMARIUM 
    cocklebur xanthium strumarium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1405
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1405-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1405-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1405-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, COCKLEBUR XANTHIUM STRUMARIUM 
    cocklebur xanthium strumarium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1408
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1408-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1408-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1408-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, COCKLEBUR XANTHIUM STRUMARIUM 
    cocklebur xanthium strumarium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1409
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1409-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1409-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1409-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, DOG FENNEL, EASTERN EUPATORIUM CAPILLIFOLIUM 
    dog fennel, eastern eupatorium capillifolium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2057
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (EUPATORIUM CAPILLIFOLIUM POLLEN - UNII:B67NF86HF0) EUPATORIUM CAPILLIFOLIUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2057-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2057-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2057-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, GOLDENROD SOLIDAGO CANADENSIS 
    goldenrod solidago canadensis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1630
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (SOLIDAGO CANADENSIS POLLEN - UNII:644CZ16IR5) SOLIDAGO CANADENSIS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1630-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1630-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1630-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, LAMBS QUARTERS CHENOPODIUM ALBUM 
    lambs quarters chenopodium album injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1786
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1786-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1786-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1786-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, LAMBS QUARTERS CHENOPODIUM ALBUM 
    lambs quarters chenopodium album injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1789
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1789-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1789-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1789-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, LAMBS QUARTERS CHENOPODIUM ALBUM 
    lambs quarters chenopodium album injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1790
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1790-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1790-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1790-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, LAMBS QUARTERS CHENOPODIUM ALBUM 
    lambs quarters chenopodium album injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1791
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1791-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1791-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1791-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, NETTLE URTICA DIOICA 
    nettle urtica dioica injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1945
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1945-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1945-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1945-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, NETTLE URTICA DIOICA 
    nettle urtica dioica injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1947
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (URTICA DIOICA POLLEN - UNII:DNB59M1NVU) URTICA DIOICA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1947-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1947-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1947-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, PIGWEED, ROUGH REDROOT AMARANTHUS RETROFLEXUS 
    pigweed, rough redroot amaranthus retroflexus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2125
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2125-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2125-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2125-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, PLANTAIN, ENGLISH PLANTAGO LANCEOLATA 
    plantain, english plantago lanceolata injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2212
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2212-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2212-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2212-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, PLANTAIN, ENGLISH PLANTAGO LANCEOLATA 
    plantain, english plantago lanceolata injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2215
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2215-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2215-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2215-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, PLANTAIN, ENGLISH PLANTAGO LANCEOLATA 
    plantain, english plantago lanceolata injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2217
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2217-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2217-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2217-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, PLANTAIN, ENGLISH PLANTAGO LANCEOLATA 
    plantain, english plantago lanceolata injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2216
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2216-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2216-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2216-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED, GIANT AMBROSIA TRIFIDA 
    ragweed, giant ambrosia trifida injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2293
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2293-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2293-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2293-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED, GIANT AMBROSIA TRIFIDA 
    ragweed, giant ambrosia trifida injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2296
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2296-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2296-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2296-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED. WESTERN AMBROSIA PSILOSTACHYA 
    ragweed. western ambrosia psilostachya injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2308
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2308-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2308-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2308-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, RAGWEED. WESTERN AMBROSIA PSILOSTACHYA 
    ragweed. western ambrosia psilostachya injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2311
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2311-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2311-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2311-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, RUSSIAN THISTLE SALSOLA KALI 
    russian thistle salsola kali injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2362
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2362-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2362-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2362-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SAGEBRUSH, MUGWORT ARTEMISIA VULGARIS 
    sagebrush, mugwort artemisia vulgaris injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2413
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2413-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2413-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2413-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SAGEBRUSH, MUGWORT ARTEMISIA VULGARIS 
    sagebrush, mugwort artemisia vulgaris injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2416
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2416-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2416-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2416-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SAGEBRUSH, MUGWORT ARTEMISIA VULGARIS 
    sagebrush, mugwort artemisia vulgaris injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2417
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2417-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2417-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2417-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SCALE, WING SHAD ATRIPLEX CANESCENS 
    scale, wing shad atriplex canescens injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2482
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2482-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2482-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2482-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SCALE, WING SHAD ATRIPLEX CANESCENS 
    scale, wing shad atriplex canescens injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2485
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (ATRIPLEX CANESCENS POLLEN - UNII:26U0BU8G83) ATRIPLEX CANESCENS POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2485-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2485-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2485-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SCOTCH BROOM CYTISUS SCOPARIUS 
    scotch broom cytisus scoparius injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2487
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666) (CYTISUS SCOPARIUS FLOWERING TOP - UNII:XZC6H8R666) CYTISUS SCOPARIUS FLOWERING TOP0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2487-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2487-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2487-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SORREL, SHEEP RUMEX ACETOSELLA 
    sorrel, sheep rumex acetosella injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2506
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2506-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2506-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2506-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS AND GARDEN PLANTS, SORREL, SHEEP RUMEX ACETOSELLA 
    sorrel, sheep rumex acetosella injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2508
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2508-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2508-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2508-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, CARELESS WEED AMARANTHUS PALMERI 
    careless weed amaranthus palmeri injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1297
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1297-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1297-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1297-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, CARELESS/PIGWEED MIX 
    careless/pigweed mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1300
    Route of AdministrationPERCUTANEOUS, 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
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1300-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1300-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1300-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, CARELESS/PIGWEED MIX 
    careless/pigweed mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1303
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH) AMARANTHUS PALMERI POLLEN0.1 g  in 1 mL
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1303-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1303-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1303-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, DOCK/SORREL MIX 
    pollens - weeds, dock/sorrel mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1516
    Route of AdministrationPERCUTANEOUS, 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
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1516-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1516-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1516-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, DOCK/SORREL MIX 
    pollens - weeds, dock/sorrel mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1519
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN0.1 g  in 1 mL
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1519-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1519-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1519-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, DOCK/SORREL MIX 
    pollens - weeds, dock/sorrel mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1520
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN20000 [PNU]  in 1 mL
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1520-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1520-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1520-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, GIANT, SHORT, WESTERN RAGWEED MIX 
    giant, short, western ragweed mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2320
    Route of AdministrationPERCUTANEOUS, 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
    AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (AMBROSIA ARTEMISIIFOLIA POLLEN - UNII:K20Y81ACO3) AMBROSIA ARTEMISIIFOLIA POLLEN0.05 g  in 1 mL
    AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (AMBROSIA PSILOSTACHYA POLLEN - UNII:RX18M46K8L) AMBROSIA PSILOSTACHYA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2320-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2320-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2320-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, KOCHIA SCOPARIA 
    kochia scoparia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1780
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1780-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1780-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1780-550 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, KOCHIA SCOPARIA 
    kochia scoparia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1783
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5) BASSIA SCOPARIA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1783-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1783-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1783-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, MARSHELDER/POVERTY MIX 
    pollens - weeds, marshelder/poverty mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1858
    Route of AdministrationPERCUTANEOUS, 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
    IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN0.05 g  in 1 mL
    CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1858-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1858-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1858-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, MARSHELDER/POVERTY MIX 
    pollens - weeds, marshelder/poverty mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1861
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IVA AXILLARIS POLLEN (UNII: 13KFG30UBR) (IVA AXILLARIS POLLEN - UNII:13KFG30UBR) IVA AXILLARIS POLLEN0.1 g  in 1 mL
    IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN0.1 g  in 1 mL
    CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1861-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1861-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1861-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, WEED MIX 2630 
    weed mix 2630 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2634
    Route of AdministrationPERCUTANEOUS, 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
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN0.05 g  in 1 mL
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN0.05 g  in 1 mL
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN0.025 g  in 1 mL
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2634-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2634-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2634-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, WEED MIX 2630 
    weed mix 2630 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2632
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN0.1 g  in 1 mL
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN0.1 g  in 1 mL
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN0.1 g  in 1 mL
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN0.05 g  in 1 mL
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2632-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2632-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2632-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, WEED MIX 2630 
    weed mix 2630 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2635
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN20000 [PNU]  in 1 mL
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN20000 [PNU]  in 1 mL
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN20000 [PNU]  in 1 mL
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN20000 [PNU]  in 1 mL
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2635-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2635-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2635-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - WEEDS, WEED MIX 2630 
    weed mix 2630 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2633
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (XANTHIUM STRUMARIUM POLLEN - UNII:2QOF601J1M) XANTHIUM STRUMARIUM POLLEN40000 [PNU]  in 1 mL
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN40000 [PNU]  in 1 mL
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN40000 [PNU]  in 1 mL
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN40000 [PNU]  in 1 mL
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2633-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2633-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2633-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - ANIMAL PRODUCTS AND POULTRY PRODUCTS, EGG, WHITE GALLUS SP. 
    egg, white gallus sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3248
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EGG WHITE (UNII: 3E0I92Z2GR) (EGG WHITE - UNII:3E0I92Z2GR) EGG WHITE0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3248-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - ANIMAL PRODUCTS AND POULTRY PRODUCTS, EGG, YOLK GALLUS SP. 
    egg, yolk gallus sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3254
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EGG YOLK (UNII: 4IPS17B70T) (EGG YOLK - UNII:4IPS17B70T) EGG YOLK0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3254-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - ANIMAL PRODUCTS AND POULTRY PRODUCTS, PORK SUS SP. 
    pork sus sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3509
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PORK (UNII: O138UB266J) (PORK - UNII:O138UB266J) PORK0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3509-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - DAIRY PRODUCTS, CASEIN, COW MILK 
    casein, cow milk injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3380
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CASEIN (UNII: 48268V50D5) (CASEIN - UNII:48268V50D5) CASEIN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3380-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - DAIRY PRODUCTS, MILK, WHOLE COW 
    milk, whole cow injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3389
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COW MILK (UNII: 917J3173FT) (COW MILK - UNII:917J3173FT) COW MILK0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3389-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, CLAM 
    clam injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3191
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUAHOG, UNSPECIFIED (UNII: 226LY0AFR9) (QUAHOG, UNSPECIFIED - UNII:226LY0AFR9) QUAHOG, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3191-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, CODFISH GADUS CALLARIAS 
    codfish gadus callarias injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3203
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COD, UNSPECIFIED (UNII: 8D6Q5LNG3D) (COD, UNSPECIFIED - UNII:8D6Q5LNG3D) COD, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3203-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, CRAB XIPHOSURUS SOWERBYI 
    crab xiphosurus sowerbyi injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3215
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CRAB LEG, UNSPECIFIED (UNII: S1VF61QLO9) (CRAB LEG, UNSPECIFIED - UNII:S1VF61QLO9) CRAB LEG, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3215-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, LOBSTER HOMARUS AMERICANUS 
    lobster homarus americanus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3362
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LOBSTER, UNSPECIFIED (UNII: ZQ6LG2C39M) (LOBSTER, UNSPECIFIED - UNII:ZQ6LG2C39M) LOBSTER, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3362-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, SALMON SALMO SALAR 
    salmon salmo salar injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3565
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALMON, UNSPECIFIED (UNII: 6122W2M0GB) (SALMON, UNSPECIFIED - UNII:6122W2M0GB) SALMON, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3565-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, SHRIMP CRAGO SP. 
    shrimp crago sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3584
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SHRIMP, UNSPECIFIED (UNII: 1891LE191T) (SHRIMP, UNSPECIFIED - UNII:1891LE191T) SHRIMP, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3584-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - FISH AND SHELLFISH, TUNA THUNNUS SP. 
    tuna thunnus sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3674
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TUNA, UNSPECIFIED (UNII: V2T3IHT3E2) (TUNA, UNSPECIFIED - UNII:V2T3IHT3E2) TUNA, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3674-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, ALMOND PRUNUS AMYGDALUS 
    almond prunus amygdalus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3014
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALMOND (UNII: 3Z252A2K9G) (ALMOND - UNII:3Z252A2K9G) ALMOND0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3014-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, APPLE MALUS SP. 
    apple malus sp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3020
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    APPLE (UNII: B423VGH5S9) (APPLE - UNII:B423VGH5S9) APPLE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3020-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, BANANA MUSA SAPIENTUM 
    banana musa sapientum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3041
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BANANA (UNII: 4AJZ4765R9) (BANANA - UNII:4AJZ4765R9) BANANA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3041-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, BRAZIL NUT BERTHOLLETIA EXCELSA 
    brazil nut bertholletia excelsa injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3107
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BRAZIL NUT (UNII: XKR79OET1K) (BRAZIL NUT - UNII:XKR79OET1K) BRAZIL NUT0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3107-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, CARROT DAUCUS CAROTA 
    carrot daucus carota injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3125
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARROT (UNII: L56Z1JK48B) (CARROT - UNII:L56Z1JK48B) CARROT0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3125-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, CASHEW NUT ANACARDIUM OCCIDENTALIE 
    cashew nut anacardium occidentalie injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3134
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CASHEW (UNII: 3H5U5CX7KO) (CASHEW - UNII:3H5U5CX7KO) CASHEW0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3134-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, CELERY APIUM GRAVEOLENS 
    celery apium graveolens injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3140
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CELERY (UNII: 44IDY6DTKX) (CELERY - UNII:44IDY6DTKX) CELERY0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3140-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, CORN ZEA MAYS 
    corn zea mays injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3212
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O) CORN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3212-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, HAZELNUT FILBERT CORYLUS SPP. 
    hazelnut filbert corylus spp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3305
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HAZELNUT, UNSPECIFIED (UNII: IW0OM96F6O) (HAZELNUT, UNSPECIFIED - UNII:IW0OM96F6O) HAZELNUT, UNSPECIFIED0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3305-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, MELON, CANTALOUPE CUCUMIS MELO 
    cantaloupe cucumis melo injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3116
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANTALOUPE (UNII: 8QF5D5H6UH) (CANTALOUPE - UNII:8QF5D5H6UH) CANTALOUPE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3116-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, ORANGE CITRUS SINENSIS 
    orange citrus sinensis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3428
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ORANGE (UNII: 5EVU04N5QU) (ORANGE - UNII:5EVU04N5QU) ORANGE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3428-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, PEA, GREEN OR ENGLISH PISUM SATIVUM 
    pea, green or english pisum sativum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3449
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PEA (UNII: W4X7H8GYFM) (PEA - UNII:W4X7H8GYFM) PEA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3449-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, PEACH PRUNUS PERSICA 
    peach prunus persica injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3452
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PEACH (UNII: 3OKE88I3QG) (PEACH - UNII:3OKE88I3QG) PEACH0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3452-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, PEANUT ARACHIS HYPOGAEA 
    peanut arachis hypogaea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3455
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PEANUT (UNII: QE1QX6B99R) (PEANUT - UNII:QE1QX6B99R) PEANUT0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3455-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, PECAN CARYA ILLINOENSIS 
    pecan carya illinoensis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3461
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PECAN (UNII: F14P91GB5F) (PECAN - UNII:F14P91GB5F) PECAN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3461-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, POTATO, WHITE SOLANUM TUBEROSUM 
    potato, white solanum tuberosum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3518
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD) POTATO0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3518-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, RICE, WHOLE GRAIN 
    rice, whole grain injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3548
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BROWN RICE (UNII: 659G217HPG) (BROWN RICE - UNII:659G217HPG) BROWN RICE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3548-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, RYE GRAIN 
    rye grain injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3554
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RYE (UNII: 0R4AQI398X) (RYE - UNII:0R4AQI398X) RYE0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3554-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, SOYBEAN GLYCINE SOJA 
    soybean glycine soja injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3596
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOYBEAN (UNII: L7HT8F1ZOD) (SOYBEAN - UNII:L7HT8F1ZOD) SOYBEAN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3596-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, STRAWBERRY FRAGARIA CHILOENSIS 
    strawberry fragaria chiloensis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3626
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STRAWBERRY (UNII: 4J2TY8Y81V) (STRAWBERRY - UNII:4J2TY8Y81V) STRAWBERRY0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3626-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, STRING BEAN MIX 
    string bean mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3074
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STRING BEAN (UNII: N9D69B2Q7Y) (STRING BEAN - UNII:N9D69B2Q7Y) STRING BEAN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3074-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, TOMATO NICOTIANA SPP. 
    tomato nicotiana spp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3656
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOMATO (UNII: Z4KHF2C175) (TOMATO - UNII:Z4KHF2C175) TOMATO0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3656-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, WALNUT, BLACK JUGLANS NIGRA 
    walnut, black juglans nigra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3695
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BLACK WALNUT (UNII: 02WM57RXZJ) (BLACK WALNUT - UNII:02WM57RXZJ) BLACK WALNUT0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3695-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, YEAST, BAKER SACCHAROMYCES CEREVISIAE 
    yeast, baker saccharomyces cerevisiae injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3713
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    YEAST (UNII: 3NY3SM6B8U) (YEAST - UNII:3NY3SM6B8U) YEAST0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3713-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    FOOD - PLANT SOURCE, YEAST, BREWER SACCHAROMYCES CEREVISIAE 
    yeast, brewer saccharomyces cerevisiae injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-3716
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    YEAST (UNII: 3NY3SM6B8U) (YEAST - UNII:3NY3SM6B8U) YEAST0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-3716-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH, AMERICAN PERIPLANETA AMERICANA 
    insects whole body cockroach, american periplaneta americana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6580
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6580-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6580-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6580-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH, GERMAN BLATELLA GERMANICA 
    insects whole body cockroach, german blatella germanica injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6581
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6581-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6581-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6581-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH MIX 
    insects whole body cockroach mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6584
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA0.1 g  in 1 mL
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6584-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6584-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6584-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH MIX 
    insects whole body cockroach mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6587
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA0.1 g  in 1 mL
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6587-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6587-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6587-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH MIX 
    insects whole body cockroach mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6588
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA20000 [PNU]  in 1 mL
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6588-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6588-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6588-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH MIX 
    insects whole body cockroach mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6589
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA20000 [PNU]  in 1 mL
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6589-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6589-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6589-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY COCKROACH MIX 
    insects whole body cockroach mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6590
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA5000 [PNU]  in 1 mL
    BLATTELLA GERMANICA (UNII: G9O67I0A8Q) (BLATTELLA GERMANICA - UNII:G9O67I0A8Q) BLATTELLA GERMANICA5000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6590-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6590-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6590-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY, FIRE ANT MIX 
    insects whole body, fire ant mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6518
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOLENOPSIS RICHTERI (UNII: 739684T11W) (SOLENOPSIS RICHTERI - UNII:739684T11W) SOLENOPSIS RICHTERI0.1 g  in 1 mL
    SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6518-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6518-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6518-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY, FIRE ANT MIX 
    insects whole body, fire ant mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6517
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOLENOPSIS RICHTERI (UNII: 739684T11W) (SOLENOPSIS RICHTERI - UNII:739684T11W) SOLENOPSIS RICHTERI0.1 g  in 1 mL
    SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6517-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-6517-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-6517-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS - ALTERNARIA/HORMODENDRUM MIX 
    molds - alternaria/hormodendrum mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5004
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.1 g  in 1 mL
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5004-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5004-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5004-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS - MOLD MIX 10 
    molds - mold mix 10 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5136
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.1 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.025 g  in 1 mL
    ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.025 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.025 g  in 1 mL
    ASPERGILLUS TERREUS (UNII: QBN8K7055X) (ASPERGILLUS TERREUS - UNII:QBN8K7055X) ASPERGILLUS TERREUS0.025 g  in 1 mL
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM0.1 g  in 1 mL
    DENDRYPHIELLA VINOSA (UNII: 7S6NW5FH8X) (DENDRYPHIELLA VINOSA - UNII:7S6NW5FH8X) DENDRYPHIELLA VINOSA0.1 g  in 1 mL
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.1 g  in 1 mL
    MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS0.1 g  in 1 mL
    PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.02 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.02 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.02 g  in 1 mL
    CLONOSTACHYS ROSEA F. ROSEA (UNII: I5F729WZ2H) (CLONOSTACHYS ROSEA F. ROSEA - UNII:I5F729WZ2H) CLONOSTACHYS ROSEA F. ROSEA0.02 g  in 1 mL
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA0.1 g  in 1 mL
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.1 g  in 1 mL
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5136-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5136-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5136-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS - MOLD MIX 4 
    molds - mold mix 4 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5000
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA0.1 g  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS0.025 g  in 1 mL
    ASPERGILLUS NIDULANS (UNII: 242A53RB80) (ASPERGILLUS NIDULANS - UNII:242A53RB80) ASPERGILLUS NIDULANS0.025 g  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.025 g  in 1 mL
    ASPERGILLUS TERREUS (UNII: QBN8K7055X) (ASPERGILLUS TERREUS - UNII:QBN8K7055X) ASPERGILLUS TERREUS0.025 g  in 1 mL
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.1 g  in 1 mL
    PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.025 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.025 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.025 g  in 1 mL
    CLONOSTACHYS ROSEA F. ROSEA (UNII: I5F729WZ2H) (CLONOSTACHYS ROSEA F. ROSEA - UNII:I5F729WZ2H) CLONOSTACHYS ROSEA F. ROSEA0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5000-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5000-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5000-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS - TRICHOPHYTON MIX 
    molds - trichophyton mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5284
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICHOPHYTON TONSURANS (UNII: JY1BE33I3Y) (TRICHOPHYTON TONSURANS - UNII:JY1BE33I3Y) TRICHOPHYTON TONSURANS0.1 g  in 1 mL
    TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N) TRICHOPHYTON RUBRUM0.1 g  in 1 mL
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5284-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5284-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5284-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, PENICILLIUM MIX 
    molds, penicillium mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5168
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (PENICILLIUM DIGITATUM - UNII:1SB49SV239) PENICILLIUM DIGITATUM0.1 g  in 1 mL
    PENICILLIUM EXPANSUM (UNII: 1XSC3BB35Z) (PENICILLIUM EXPANSUM - UNII:1XSC3BB35Z) PENICILLIUM EXPANSUM0.1 g  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM0.1 g  in 1 mL
    CLONOSTACHYS ROSEA F. ROSEA (UNII: I5F729WZ2H) (CLONOSTACHYS ROSEA F. ROSEA - UNII:I5F729WZ2H) CLONOSTACHYS ROSEA F. ROSEA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5168-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5168-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5168-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5008
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5008-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5008-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5008-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5020
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5020-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5020-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5020-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, ASPERGILLUS NIGER 
    aspergillus niger injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5032
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5032-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5032-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5032-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5048
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5048-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5048-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5048-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    INSECTS WHOLE BODY, ANT, FIRE SOLENOPSIS INVICTA 
    ant, fire solenopsis invicta injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-6513
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-6513-210 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5052
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5052-110 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5052-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5052-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5055
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5055-110 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5055-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5055-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, CEPHALOSPORIUM ACREMONIUM 
    cephalosporium acremonium injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5056
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5056-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5056-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5056-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, CURVULARIA SPICIFERA 
    curvularia spicifera injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5076
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (COCHLIOBOLUS SPICIFER - UNII:91M9RWP3TD) COCHLIOBOLUS SPICIFER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5076-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5076-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5076-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5100
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5100-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5100-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5100-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, EPIDERMOPHYTON FLOCCOSUM 
    epidermophyton floccosum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5104
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (EPIDERMOPHYTON FLOCCOSUM - UNII:6JR6JTN25S) EPIDERMOPHYTON FLOCCOSUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5104-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5104-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5104-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, FUSARIUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5112
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5112-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5112-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5112-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, HELMINTHOSPORIUM INTERSEMINATUM 
    helminthosporium interseminatum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5124
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DENDRYPHIELLA VINOSA (UNII: 7S6NW5FH8X) (DENDRYPHIELLA VINOSA - UNII:7S6NW5FH8X) DENDRYPHIELLA VINOSA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5124-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5124-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5124-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, HORMODENDRUM CLADOSPORIOIDES 
    hormodendrum cladosporioides injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5128
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5128-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5128-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5128-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, MUCOR RACEMOSUS 
    mucor racemosus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5144
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5144-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5144-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5144-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, PENICILLIUM NOTATUM 
    penicillium notatum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5208
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5208-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5208-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5208-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, PHOMA HERBARUM 
    phoma herbarum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5220
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5220-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5220-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5220-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, PULLULARIA PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5235
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5235-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5235-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5235-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, RHIZOPUS NIGRICANS 
    rhizopus nigricans injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5230
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (RHIZOPUS STOLONIFER - UNII:FEE198DK4Q) RHIZOPUS STOLONIFER0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5230-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5230-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5230-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    MOLDS, RUSTS AND SMUTS, STEMPHYLIUM BOTRYOSUM 
    stemphylium botryosum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-5264
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-5264-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-5264-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-5264-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, BAHIA GRASS PASPALUM NOTATUM 
    bahia grass paspalum notatum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1081
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1081-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1081-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1081-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, BAHIA GRASS PASPALUM NOTATUM 
    bahia grass paspalum notatum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1084
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1084-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1084-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1084-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, BROME, SMOOTH BROMUS INERMIS 
    brome, smooth bromus inermis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1237
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1237-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1237-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1237-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, CORN, CULTIVATED ZEA MAYS 
    corn, cultivated zea mays injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1414
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1414-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1414-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1414-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, JOHNSON GRASS SORGHUM HALEPENSE 
    johnson grass sorghum halepense injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1744
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1744-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1744-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1744-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, JOHNSON GRASS SORGHUM HALEPENSE 
    johnson grass sorghum halepense injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1747
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1747-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1747-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1747-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, OATS, COMMON, CULTIVATED AVENA SATIVA 
    oats, common, cultivated avena sativa injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2041
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2041-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2041-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2041-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, GRASS MIX 8 
    grass mix 8 injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-0879
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (POA PRATENSIS POLLEN - UNII:SCB8J7LS3T) POA PRATENSIS POLLEN100000 [BAU]  in 1 mL
    CYNODON DACTYLON POLLEN (UNII: 175F461W10) (CYNODON DACTYLON POLLEN - UNII:175F461W10) CYNODON DACTYLON POLLEN10000 [BAU]  in 1 mL
    SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN0.05 g  in 1 mL
    AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (AGROSTIS GIGANTEA POLLEN - UNII:HU8V6E7HOA) AGROSTIS GIGANTEA POLLEN100000 [BAU]  in 1 mL
    PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (PHLEUM PRATENSE POLLEN - UNII:65M88RW2EG) PHLEUM PRATENSE POLLEN100000 [BAU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-0879-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, SOUTHERN GRASS MIX 
    pollens - grasses, southern grass mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-0854
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (POA PRATENSIS POLLEN - UNII:SCB8J7LS3T) POA PRATENSIS POLLEN100000 [BAU]  in 1 mL
    DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P) (DACTYLIS GLOMERATA POLLEN - UNII:83N78IDA7P) DACTYLIS GLOMERATA POLLEN100000 [BAU]  in 1 mL
    AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (AGROSTIS GIGANTEA POLLEN - UNII:HU8V6E7HOA) AGROSTIS GIGANTEA POLLEN100000 [BAU]  in 1 mL
    PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (PHLEUM PRATENSE POLLEN - UNII:65M88RW2EG) PHLEUM PRATENSE POLLEN100000 [BAU]  in 1 mL
    ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (ANTHOXANTHUM ODORATUM POLLEN - UNII:2KIK19R45Y) ANTHOXANTHUM ODORATUM POLLEN100000 [BAU]  in 1 mL
    SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN0.05 g  in 1 mL
    CYNODON DACTYLON POLLEN (UNII: 175F461W10) (CYNODON DACTYLON POLLEN - UNII:175F461W10) CYNODON DACTYLON POLLEN10000 [BAU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-0854-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-0854-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-0854-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - GRASSES, SOUTHERN GRASS MIX 
    pollens - grasses, southern grass mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-0856
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (POA PRATENSIS POLLEN - UNII:SCB8J7LS3T) POA PRATENSIS POLLEN10000 [BAU]  in 1 mL
    DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P) (DACTYLIS GLOMERATA POLLEN - UNII:83N78IDA7P) DACTYLIS GLOMERATA POLLEN10000 [BAU]  in 1 mL
    AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (AGROSTIS GIGANTEA POLLEN - UNII:HU8V6E7HOA) AGROSTIS GIGANTEA POLLEN10000 [BAU]  in 1 mL
    PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (PHLEUM PRATENSE POLLEN - UNII:65M88RW2EG) PHLEUM PRATENSE POLLEN10000 [BAU]  in 1 mL
    ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (ANTHOXANTHUM ODORATUM POLLEN - UNII:2KIK19R45Y) ANTHOXANTHUM ODORATUM POLLEN10000 [BAU]  in 1 mL
    SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN0.005 g  in 1 mL
    CYNODON DACTYLON POLLEN (UNII: 175F461W10) (CYNODON DACTYLON POLLEN - UNII:175F461W10) CYNODON DACTYLON POLLEN1000 [BAU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-0856-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-0856-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-0856-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ACACIA ACACIA LONGIFOLIA 
    acacia longifolia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1006
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACACIA LONGIFOLIA POLLEN (UNII: 24SO2J296O) (ACACIA LONGIFOLIA POLLEN - UNII:24SO2J296O) ACACIA LONGIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1006-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1006-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1006-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ALDER, RED ALNUS RUBRA 
    alder, red alnus rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1018
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1018-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1018-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1018-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ALDER, RED ALNUS RUBRA 
    alder, red alnus rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1021
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (ALNUS RUBRA POLLEN - UNII:Z0F2YK1B7H) ALNUS RUBRA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1021-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1021-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1021-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ASH, WHITE FRAXINUS AMERICANA 
    ash, white fraxinus americana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1060
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1060-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1060-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1060-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BEECH, AMERICAN FAGUS GRANDIFOLIA 
    beech, american fagus grandifolia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1120
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1120-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1120-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1120-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BIRCH MIX 
    birch mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1168
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN0.05 g  in 1 mL
    BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN0.05 g  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1168-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1168-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1168-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BIRCH MIX 
    birch mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1171
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN0.1 g  in 1 mL
    BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN0.1 g  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1171-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1171-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1171-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BIRCH MIX 
    birch mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1172
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (BETULA PAPYRIFERA POLLEN - UNII:3538FNV8AY) BETULA PAPYRIFERA POLLEN20000 [PNU]  in 1 mL
    BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (BETULA PENDULA POLLEN - UNII:ZL5TV40C5Y) BETULA PENDULA POLLEN40000 [PNU]  in 1 mL
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1172-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1172-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1172-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BOTTLE BRUSH CALLISTEMON SPP. 
    bottle brush callistemon spp. injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1207
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELALEUCA CITRINA POLLEN (UNII: 62OII98F1T) (MELALEUCA CITRINA POLLEN - UNII:62OII98F1T) MELALEUCA CITRINA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1207-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1207-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1207-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BOXELDER/MAPLE MIX 
    boxelder/maple mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1213
    Route of AdministrationPERCUTANEOUS, 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
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.05 g  in 1 mL
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1213-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1213-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1213-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BOXELDER/MAPLE MIX 
    boxelder/maple mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1216
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN0.1 g  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN0.1 g  in 1 mL
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1216-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1216-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1216-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, BOXELDER/MAPLE MIX 
    boxelder/maple mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1217
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN40000 [PNU]  in 1 mL
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN40000 [PNU]  in 1 mL
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1217-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1217-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1217-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, CEDAR, MOUNTAIN JUNIPERUS ASHEI 
    cedar, mountain juniperus ashei injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1336
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1336-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1336-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1336-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, CEDAR, MOUNTAIN JUNIPERUS ASHEI 
    cedar, mountain juniperus ashei injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1339
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1339-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1339-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1339-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, CEDAR, RED JUNIPERUS VIRGINIANA 
    cedar, red juniperus virginiana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1343
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1343-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1343-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1343-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, CEDAR, RED JUNIPERUS VIRGINIANA 
    cedar, red juniperus virginiana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1342
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1342-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1342-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1342-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, COTTONWOOD, COMMON POPULUS DELTOIDES 
    cottonwood, common populus deltoides injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1435
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1435-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1435-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1435-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, COTTONWOOD, COMMON POPULUS DELTOIDES 
    cottonwood, common populus deltoides injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1438
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1438-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1438-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1438-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, CYPRESS, ARIZONA CUPRESSUS ARIZONICA 
    cypress, arizona cupressus arizonica injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1450
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1450-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1450-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1450-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, CYPRESS, BALD TAXODIUM DISTICHUM 
    cypress, bald taxodium distichum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1453
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TAXODIUM DISTICHUM POLLEN (UNII: O12H03B41R) (TAXODIUM DISTICHUM POLLEN - UNII:O12H03B41R) TAXODIUM DISTICHUM POLLEN0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1453-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1453-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1453-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ELM, AMERICAN ULMUS AMERICANA 
    elm, american ulmus americana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1540
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1540-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1540-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1540-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ELM, AMERICAN ULMUS AMERICANA 
    elm, american ulmus americana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1543
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1543-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1543-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1543-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ELM, AMERICAN ULMUS AMERICANA 
    elm, american ulmus americana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1544
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1544-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1544-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1544-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, ELM, CHINESE ULMUS PARVIFOLIA 
    elm, chinese ulmus parvifolia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1546
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ULMUS PARVIFOLIA POLLEN (UNII: IU0Z41653U) (ULMUS PARVIFOLIA POLLEN - UNII:IU0Z41653U) ULMUS PARVIFOLIA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1546-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1546-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1546-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, EUCALYPTUS, EUCALYPTUS GLOBULUS 
    eucalyptus, eucalyptus globulus injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1564
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1564-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1564-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1564-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, GUM, SWEET LIQUIDAMBAR STYRACIFLUA 
    gum, sweet liquidambar styraciflua injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1660
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1660-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1660-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1660-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, GUM, SWEET LIQUIDAMBAR STYRACIFLUA 
    gum, sweet liquidambar styraciflua injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1662
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS) LIQUIDAMBAR STYRACIFLUA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1662-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1662-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1662-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, HACKBERRY CELTIS OCCIDENTALIS 
    hackberry celtis occidentalis injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1663
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1663-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1663-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1663-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, HICKORY, SHAGBARK CARYA OVATA 
    hickory, shagbark carya ovata injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1702
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1702-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1702-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1702-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, LINDEN BASSWOOD TILIA AMERICANA 
    linden basswood tilia americana injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1801
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TILIA AMERICANA POLLEN (UNII: E2B4Q4BXJG) (TILIA AMERICANA POLLEN - UNII:E2B4Q4BXJG) TILIA AMERICANA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1801-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1801-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1801-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, MAPLE, HARD ACER SACCHARUM 
    maple, hard acer saccharum injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1831
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1831-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1831-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1831-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, MELALEUCA PUNK TREE MELALEUCA QUINQUENERVIA 
    melaleuca punk tree melaleuca quinquenervia injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1873
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1873-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1873-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1873-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, MESQUITE, PROSOPIS JULIFLORA 
    mesquite, prosopis juliflora injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1876
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1876-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1876-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1876-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, MULBERRY MIX 
    mulberry mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1909
    Route of AdministrationPERCUTANEOUS, 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
    MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1909-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1909-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1909-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, MULBERRY MIX 
    mulberry mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-1912
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN0.1 g  in 1 mL
    MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-1912-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-1912-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-1912-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, OAK MIX 
    oak mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2035
    Route of AdministrationPERCUTANEOUS, 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
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN0.05 g  in 1 mL
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2035-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2035-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2035-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, OAK MIX 
    oak mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2038
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN0.1 g  in 1 mL
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN0.1 g  in 1 mL
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN0.1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2038-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2038-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2038-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, OAK MIX 
    oak mix injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2039
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN20000 [PNU]  in 1 mL
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN20000 [PNU]  in 1 mL
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2039-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2039-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2039-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, OAK, RED QUERCUS RUBRA 
    oak, red quercus rubra injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2014
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2014-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2014-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2014-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    POLLENS - TREES, OLIVE OLEA EUROPAEA 
    olive olea europaea injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-2050
    Route of AdministrationPERCUTANEOUS, 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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65044-2050-210 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:65044-2050-330 mL in 1 VIAL; Type 0: Not a Combination Product
    3NDC:65044-2050-450 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10388804/19/1941
    ANIMAL ALLERGENS, UF DOG HAIR-DANDER CANIS SPP 
    animal allergens, dog dander canis spp injection, solution
    Product Information
    Product TypeNON-STANDARDIZED ALLERGENICItem Code (Source)NDC:65044-4850
    Route of AdministrationPERCUTANEOUS, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (CANIS LUPUS FAMILIARIS HAIR - UNII:05S7L91ZTR) CANIS LUPUS FAMILIARIS HAIR0.0008 g  in 1 mL
    CANIS LUPUS FAMILIARIS DANDER (UNII: 11JCK302I4) (CANIS LUPUS FAMILIARIS DANDER - UNII:11JCK302I4) CANIS LUPUS FAMILIARIS DANDER0.0008 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging