Label: ASPERSAN- aspergillus niger var. niger liquid

  • 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 September 9, 2019

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

  • Indications

    For lymphatic stagnation

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  • Dosage

    5-10 drops, three times daily.

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  • Ingredients

    10ml Aspergillus niger 4X in a base of purified water, 0.09g sodium chloride, 0.01g potassium sorbate.

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  • Warning

    If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.

    Keep this and all medications out of the reach of children.

    Protect from light and heat.

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  • Tamper Evident

    Do not use product if tamper evident strip is broken or removed from base of cap.

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  • QUESTIONS

    To report adverse events, contact BioResource at 707/664-9023 or bioresource2@prodigy.net

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  • SPL UNCLASSIFIED SECTION

    Distributed By:
    BioResource Inc.
    Cotati CA 94931

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  • PRINCIPAL DISPLAY PANEL - 10 ml Bottle Carton

    AsperSAN

    Homeopathic
    Medicine

    For lymphatic
    stagnation

    0.34 FL OZ
    (10ml)

    san Pharma ®
    biological health solutions

    PRINCIAP DISPLAY PANEL - AsperSAN Drops

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  • INGREDIENTS AND APPEARANCE
    ASPERSAN 
    aspergillus niger var. niger liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:64232-030
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 4 [hp_X]  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64232-030-17 1 in 1 CARTON 01/04/2017
    1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/04/2017
    Labeler - sanPharma GmbH (341409153)
    Establishment
    Name Address ID/FEI Business Operations
    sanPharma GmbH 341409153 manufacture(64232-030) , label(64232-030)
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