Label: ASPERGILLUS- 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 January 29, 2016

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  • Indications

    For treatment of lymphatic stagnation.

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  • Ingredients

    182 mg 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.

    Tamper Evident

    Use this product only if inner blister pack is intact.

    To report adverse events, contact BioResource at 707/664-9023 or bioresource@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

    SanPharma™
    Aspergillus
    Suppositories 3X

    Homeopathic
    Medicine

    For lymphatic stagnation

    RX

    10 SUPPOSITORIES

    SanPharma ™

    PRINCIPAL DISPLAY PANEL - 10 Suppository Blister Pack Box
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  • INGREDIENTS AND APPEARANCE
    ASPERGILLUS 
    aspergillus niger var. niger suppository
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:54256-029
    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)  
    Sodium chloride (UNII: 451W47IQ8X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:54256-029-04 1 in 1 BOX
    1 10 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 10/10/2015
    Labeler - BioResource Inc. (017532917)
    Establishment
    Name Address ID/FEI Business Operations
    RubiePharm Arzneimittel GmbH 313767774 MANUFACTURE(54256-029)
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