Label: PRUNUS SPINOSA E SUMM 10% liquid

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated April 30, 2018

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

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

  • ACTIVE INGREDIENT


    Active Ingredient: 100 gm contains: 10gm Prunus spinosa (Blackthorn) 1X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Organic cane alcohol

  • PURPOSE

    Use: Temporary relief of fatigue.

  • 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. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858
    Made with care by Uriel, East Troy, WI 53120
    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    PrunusSpinosaESumm10Liquid

  • INGREDIENTS AND APPEARANCE
    PRUNUS SPINOSA E SUMM 10% 
    prunus spinosa e summ 10% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8082
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PRUNUS SPINOSA WHOLE (UNII: 5342MY2M3P) (PRUNUS SPINOSA WHOLE - UNII:5342MY2M3P) PRUNUS SPINOSA WHOLE10 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8082-31 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
    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(48951-8082)