Label: PRUNUS SPINOSA E SUMM 10%- prunus spinosa whole 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 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 LABEL 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 (PRUNUS SPINOSA WHOLE) PRUNUS SPINOSA WHOLE 10 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    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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