Quercus 5 by Uriel Pharmacy Inc. QUERCUS 5 ointment

Quercus 5 by

Drug Labeling and Warnings

Quercus 5 by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION

Apply to skin as needed. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredient: 100 gm contains: 5 gm Quercus (Oak) 1X

INACTIVE INGREDIENT

Inactive Ingredients: Lanolin, Organic olive oil, Distilled water, Beeswax, Glyceryl monostearate, Stearyl alcohol, Potassium sorbate, Polyoxyl 40 stearate, Grapefruit seed extract

PURPOSE

Use: Temporary relief of rash.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: FOR EXTERNAL USE ONLY.
Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. 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

INGREDIENTS AND APPEARANCE

QUERCUS 5 
quercus 5 ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-8113
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W)	QUERCUS ROBUR WHOLE	1 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
OLIVE OIL (UNII: 6UYK2W1W1E)
WATER (UNII: 059QF0KO0R)
YELLOW WAX (UNII: 2ZA36H0S2V)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
CITRUS PARADISI SEED (UNII: 12F08874Y7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-8113-5	60 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009

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(48951-8113)