Label: PRUNUS SPINOSA E SUMM 10%- prunus spinosa whole liquid

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

Drug Label Information

Updated 11/13

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

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  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 10 drops.
    Ages 2-11: 5 drops. Under age 2: Consult a doctor.

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  • ACTIVE INGREDIENT


    Active Ingredient: 100 gm contains: 10gm Prunus spinosa e summ. MT

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Organic cane alcohol

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  • PURPOSE

    Use: Temporary relief of fatigue.

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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. 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
    Made with care by Uriel, East Troy, WI 53120
    www.urielpharmacy.com

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  • INGREDIENTS AND APPEARANCE
    PRUNUS SPINOSA E SUMM 10% 
    prunus spinosa e summ 10% liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8082
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PRUNUS SPINOSA WHOLE (UNII: 5342MY2M3P) (PRUNUS SPINOSA WHOLE - UNII:5342MY2M3P) PRUNUS SPINOSA WHOLE 10 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-8082-3 1 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(48951-8082)
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