PRUNUS SPINOSA E FLOR. ET SUMM. 2- prunus spinosa e flor. et summ. 2 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.

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Prunus spinosa e flor. et summ. 2

Directions: FOR ORAL USE.

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Active Ingredient: Prunus spinosa e flor. et summ. (Blackthorn) 2X

Inactive Ingredients: Water, Salt

Use: Temporary relief of fatigue.

KEEP OUT OF REACH OF CHILDREN.

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.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

PrunusSpinosaEFlorEtSumm2Ampules

PRUNUS SPINOSA E FLOR. ET SUMM. 2
prunus spinosa e flor. et summ. 2 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-8078
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W) (PRUNUS SPINOSA FLOWER BUD - UNII:53Y84VPS2W)	PRUNUS SPINOSA FLOWER BUD	2 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-8078-1	10 in 1 BOX	09/01/2009	10/13/2020
1		1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	10/13/2020

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-8078)

Revised: 12/2020

Document Id: b5e35ca1-1673-879c-e053-2a95a90aff00

Set id: b9d83abf-de7b-4543-acb4-7abc1865644a

Version: 4

Effective Time: 20201207

Uriel Pharmacy Inc.