Label: LYCOPODIUM BERBERIS- lycopodium berberis liquid

  • Category: HUMAN OTC DRUG LABEL

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 May 23, 2018

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE.

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  • DOSAGE & ADMINISTRATION

    Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

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  • ACTIVE INGREDIENT

    Active Ingredients: Berberis (Barberry) 3X,
    Carduus marianus (Milk thistle) 4X, Chelidonium (Greater celandine) 5X, Curcuma (Turmeric) 5X, Fragaria (Wild strawberry) 5X, Lycopodium (Club moss) 5X, Vitis vinif. (Grape vine) 5X, Natrium sulf. (Sodium sulfate) 6X, Mercurius dulcis (Mercurous chloride) 10X

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt

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  • PURPOSE

    Use: Temporary relief of digestive upset.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

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  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

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  • QUESTIONS

    Questions? Call 866.642.2858
    Made by Uriel, East Troy, WI 53120
    www.urielpharmacy.com

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  • INGREDIENTS AND APPEARANCE
    LYCOPODIUM BERBERIS 
    lycopodium berberis liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-6048
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 3 [hp_X]  in 1 mL
    MILK THISTLE (UNII: U946SH95EE) (MILK THISTLE - UNII:U946SH95EE) MILK THISTLE 4 [hp_X]  in 1 mL
    CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N) (CHELIDONIUM MAJUS ROOT - UNII:FLT36UCF0N) CHELIDONIUM MAJUS ROOT 5 [hp_X]  in 1 mL
    TURMERIC (UNII: 856YO1Z64F) (TURMERIC - UNII:856YO1Z64F) TURMERIC 5 [hp_X]  in 1 mL
    FRAGARIA VESCA WHOLE (UNII: 5J340B7H82) (FRAGARIA VESCA WHOLE - UNII:5J340B7H82) FRAGARIA VESCA WHOLE 5 [hp_X]  in 1 mL
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 5 [hp_X]  in 1 mL
    VITIS VINIFERA LEAF (UNII: R1H893D80E) (VITIS VINIFERA LEAF - UNII:R1H893D80E) VITIS VINIFERA LEAF 5 [hp_X]  in 1 mL
    SULFIDE ION (UNII: G15I91XETI) (SULFIDE ION - UNII:G15I91XETI) SULFIDE ION 6 [hp_X]  in 1 mL
    CALOMEL (UNII: J2D46N657D) (CALOMEL - UNII:J2D46N657D) CALOMEL 10 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-6048-1 10 in 1 BOX 09/01/2009
    1 1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    Uriel Pharmacy Inc. 043471163 manufacture(48951-6048)
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