Label: APIS BELLADONNA MERCURIUS- atropa belladonna, apis mellifera and mercurius solubilis pellet

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

Drug Label Information

Updated 03/14

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

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  • DOSAGE & ADMINISTRATION

    ´╗┐Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

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  • ACTIVE INGREDIENT

    Active Ingredients: Atropa belladonna
    ex herba 4X, Apis ex animale 5X,
    Mercurius solubilis 17X

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  • INACTIVE INGREDIENT

    ´╗┐Inactive Ingredient: Sucrose

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  • PURPOSE

    Use: Temporary relief of sore throat.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

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  • WARNINGS

    Warnings: Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing. 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 BELLADONNA MERCURIUS 
    apis belladonna mercurius pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1049
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 4 [hp_X]
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 5 [hp_X]
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 17 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Color white Score     
    Shape capsule Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-1049-2 1350 in 1 BOTTLE, GLASS
    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(48951-1049)
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