Label: A-22- aspergillus flavus, aspergillus fumigatus, eurotium herbariorum, aspergillus nidulans, aspergillus niger var. niger, penicillium camemberti, penicillium chrysogenum var. chrysogenum, penicillium digitatum, and penicillium roqueforti solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated February 12, 2018

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

  • SPL UNCLASSIFIED SECTION

    NDC 58264-0314-1

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  • INDICATIONS

    Allergies.

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  • INGREDIENTS

    Aspergillus: Flavus 6/12/30x, Fumigatus 6/12/30x, Glaucus 6/12/30x, Nidulans 6/12/30x, Niger 6/12/30x, Penicillium: Camemberti 6/12/30x, Chrysogenum 6/12/30x, Digitatum 6/12/30x, Notatum 6/12/30x, Roqueforti 6/12/30x, 20% alcohol in purified water.

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  • SUGGESTED DOSAGE

    Normal dose for the first week is 2-3 drops in water T.I.D. Add one drop per dose per week until a total of ten drops is reached.

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  • STORAGE AND HANDLING

    SHAKE WELL

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  • Warnings

    • Use only if cap seal is unbroken.

    • As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.

    • Keep this and all medication out of the reach of children.
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  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

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  • PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

    DYNAMIC
    NUTRITIONAL

    ASSOCIATES, INC.

    A-22
    MOLD MIX #2

    HOMEOPATHIC ANTIGEN

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    A-22 
    aspergillus flavus, aspergillus fumigatus, eurotium herbariorum, aspergillus nidulans, aspergillus niger var. niger, penicillium camemberti, penicillium chrysogenum var. chrysogenum, penicillium digitatum, and penicillium roqueforti solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0314
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (Aspergillus Flavus - UNII:3J888Y9L13) ASPERGILLUS FLAVUS 30 [hp_X]  in 1 mL
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Aspergillus Fumigatus - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 30 [hp_X]  in 1 mL
    EUROTIUM HERBARIORUM (UNII: 49W168AES4) (EUROTIUM HERBARIORUM - UNII:49W168AES4) EUROTIUM HERBARIORUM 30 [hp_X]  in 1 mL
    ASPERGILLUS NIDULANS (UNII: 242A53RB80) (Aspergillus Nidulans - UNII:242A53RB80) ASPERGILLUS NIDULANS 30 [hp_X]  in 1 mL
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 30 [hp_X]  in 1 mL
    PENICILLIUM CAMEMBERTI (UNII: T069R9OPVG) (Penicillium Camemberti - UNII:T069R9OPVG) PENICILLIUM CAMEMBERTI 30 [hp_X]  in 1 mL
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 30 [hp_X]  in 1 mL
    PENICILLIUM DIGITATUM (UNII: 1SB49SV239) (Penicillium Digitatum - UNII:1SB49SV239) PENICILLIUM DIGITATUM 30 [hp_X]  in 1 mL
    PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (Penicillium Roqueforti - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI 30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:58264-0314-1 29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    UNAPPROVED HOMEOPATHIC 01/01/1990
    Labeler - DNA Labs, Inc. (031784339)
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