VISCUM PINI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]

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VISCUM PINI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]
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NDC 48951-1004-1
Set ID 03ba9cf0-46c0-416a-b5bf-11ea5b5cdc4f
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc
Generic Name
Product Class
Product Number
Application Number
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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE.

  • DOSAGE & ADMINISTRATION

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

  • ACTIVE INGREDIENT

    Active Ingredient: Viscum album (Pini)1 gm contains:
    A13X 93.7%
    B10X 37.5%
    C7X 15.6%
    D6X 31.2%
    E5X 62.5%
    F3X 12.5%
    G2X 25%
  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • 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.

  • QUESTIONS

    Questions? Call 866 642-2858

    Uriel, East Troy, WI 53120

    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    ViscumPiniAAmpulesViscumPiniBAmpulesViscumPiniCAmpulesViscumPiniDAmpulesViscumPiniEAmpulesViscumPiniFAmpulesViscumPiniGAmpules

  • INGREDIENTS AND APPEARANCE
    VISCUM PINI 
    viscum album fruiting top liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1004
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP2 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1004-110 in 1 PACKAGE09/01/2009
    11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc043471163manufacture(48951-1004)
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