Label: ASPERSAN- aspergillus niger var. niger suppository

  • 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 March 7, 2019

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

  • Indications

    For lymphatic stagnation.

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  • Ingredients

    182mg Aspergillus niger 3X with sodium chloride in a base of mono-, di-, triglycerides (hard fat).

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  • Dosage

    Insert one suppository rectally each night before bed.

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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

    Use this product only if inner blister pack is intact. 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 Suppository Blister Pack Box

    AsperSAN

    Homeopathic Medicine

    For lymphatic stagnation

    10 Suppositories

    sanPharma ®
    biological health solutions

    PRINCIPAL DISPLAY PANEL - 10 Suppository Blister Pack Box
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  • INGREDIENTS AND APPEARANCE
    ASPERSAN 
    aspergillus niger var. niger suppository
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:64232-029
    Route of Administration RECTAL
    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 3 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    FAT, HARD (UNII: 8334LX7S21)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64232-029-17 2 in 1 BOX 12/01/2017
    1 5 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 12/01/2017
    Labeler - sanPharma GmbH (341409153)
    Establishment
    Name Address ID/FEI Business Operations
    sanPharma GmbH 341409153 manufacture(64232-029) , label(64232-029)
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