VISCUM CRATAEGI SERIES 1 LIQUID [URIEL PHARMACY INC.]

VISCUM CRATAEGI SERIES 1 LIQUID [URIEL PHARMACY INC.]
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NDC 48951-9207-1
Set ID 7f679f06-d795-4a61-9f18-4bba60943943
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
  • 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 - Crataegi (Hawthorn tree mistletoe)

    3 amps St. A = 1 gm contains: 13X, 93.7%

    3 amps St. B = 1 gm contains: 10X, 37.5%

    3 amps St. C = 1 gm contains: 7X, 15.6%

    1 amp St. D = 1 gm contains: 6X, 31.2%

  • 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 homepathic 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

    ViscumCrataegiIscucinSeries1Ampules

  • INGREDIENTS AND APPEARANCE
    VISCUM CRATAEGI SERIES 1 
    viscum crataegi series 1 liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-9207
    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 TOP6 [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:48951-9207-110 in 1 PACKAGE, COMBINATION09/01/2009
    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 Inc.043471163manufacture(48951-9207)

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