Label: VISCUM ABIETIS- viscum album fruiting top liquid

  • 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 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 LABEL 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 (VISCUM ALBUM FRUITING TOP) VISCUM ALBUM FRUITING TOP 2 [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:48951-1001-1 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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