Label: VISCUM ABIETIS- viscum album fruiting top liquid

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

Drug Label Information

Updated 01/13

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  • DOSAGE & ADMINISTRATION

    Directions: FOR ORAL USE ONLY. Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

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  • ACTIVE INGREDIENT

    Active Ingredient: Viscum album (Abietis) 1 gm contains:
    A 13X 93.7%
    B 10X 37.5%
    C 7X 15.6%
    D 6X 31.2%
    E 5X 62.5%
    F 3X 12.5%
    G 2X 25%
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  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt

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  • INDICATIONS & USAGE

    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.

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  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or nursing, consult a doctor before use.

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  • SPL UNCLASSIFIED SECTION

    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
    VISCUM ABIETIS 
    viscum album fruiting top liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1001
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP 2 [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:48951-1001-1 10 in 1 PACKAGE
    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(48951-1001)
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