Prunus Spinosa E Summ 30: Homeopathic Product Information

PRUNUS SPINOSA E SUMM 30- sloe liquid
Uriel Pharmacy Inc.

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.

Directions: FOR ORAL USE ONLY.

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

Active Ingredient: 100 gm contains: 30gm Prunus spinosa e summ. (Blackthorn) 1X

Inactive Ingredients: Distilled water, 30% Organic cane alcohol

Use: Temporary relief of fatigue.


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? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120

Prunus spinosa e summ. 30 Liquid

prunus spinosa e summ 30 liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8376
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SLOE (SLOE) SLOE 1 [hp_X] in 1 mL
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:48951-8376-3 60 mL in 1 BOTTLE, DROPPER None
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)
Name Address ID/FEI Operations
Uriel Pharmacy Inc. 043471163 manufacture (48951-8376)

Revised: 07/2021 Uriel Pharmacy Inc. provides trustworthy package insert and label information about marketed homeopathic remedies as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

We source our database directly from the FDA's central repository of homeopathic remedy labels and package inserts, under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

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