Label: APIS GELSEMIUM- berberis vulgaris root bark, gelsemium sempervirens root, apis mellifera, pseudognaphalium luteoalbum leaf, colchicum autumnale flower, formica rufa and arnica montana root liquid 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 03/14

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

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

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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 e rad.
    3X, Gelsemium e rad. 3X, Apis ex
    animale 4X, Gnaphalium e pl. tota
    4X, Colchicum e pl. tota 5X, Formica
    ex animale 5X, Arnica e rad. 10X

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt

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  • PURPOSE

    Use: Temporary relief of headache.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

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  • WARNINGS

    Warnings: 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. Natural

    ingredients may cause color, scent and/or taste variation.

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  • QUESTIONS


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

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  • INGREDIENTS AND APPEARANCE
    APIS GELSEMIUM 
    apis gelsemium liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:48951-1057
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BERBERIS VULGARIS ROOT BARK (BERBERIS VULGARIS ROOT BARK) BERBERIS VULGARIS ROOT BARK 3 [hp_X]  in 1 mL
    GELSEMIUM SEMPERVIRENS ROOT (GELSEMIUM SEMPERVIRENS ROOT) GELSEMIUM SEMPERVIRENS ROOT 3 [hp_X]  in 1 mL
    APIS MELLIFERA (APIS MELLIFERA) APIS MELLIFERA 4 [hp_X]  in 1 mL
    PSEUDOGNAPHALIUM LUTEOALBUM LEAF (PSEUDOGNAPHALIUM LUTEOALBUM LEAF) PSEUDOGNAPHALIUM LUTEOALBUM LEAF 4 [hp_X]  in 1 mL
    COLCHICUM AUTUMNALE FLOWER (COLCHICUM AUTUMNALE FLOWER) COLCHICUM AUTUMNALE FLOWER 5 [hp_X]  in 1 mL
    FORMICA RUFA (FORMICA RUFA) FORMICA RUFA 5 [hp_X]  in 1 mL
    ARNICA MONTANA ROOT (ARNICA MONTANA ROOT) ARNICA MONTANA ROOT 10 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM CHLORIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-1057-1 10 in 1 BOX
    1 1 mL in 1 AMPULE
    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(48951-1057)
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