Onopordon Aurum by Uriel Pharmacy, Inc. ONOPORDON AURUM liquid

Onopordon Aurum by

Drug Labeling and Warnings

Onopordon Aurum 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 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 Ingredients: 100gm contains: 2.5gm Onopordon (Cotton thistle) 1X, 2.5gm Primula (Cowslip) 1X; Hyoscyamus (Henbane) 3X, Aurum met. (Metallic gold) 10X

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, 30% Organic cane alcohol

Prepared using rhythmical processes.

PURPOSE

Use: Promotes healthy circulatory support.

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
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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ONOPORDON AURUM 
onopordon aurum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-7210
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYOSCYAMUS NIGER LEAF (UNII: 32IT7G8BAW) (HYOSCYAMUS NIGER LEAF - UNII:32IT7G8BAW)	HYOSCYAMUS NIGER LEAF	3 [hp_X]  in 1 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	10 [hp_X]  in 1 mL
ONOPORDUM ACANTHIUM FLOWER (UNII: AP97AUF88E) (ONOPORDUM ACANTHIUM FLOWER - UNII:AP97AUF88E)	ONOPORDUM ACANTHIUM FLOWER	1 [hp_X]  in 1 mL
PRIMULA VERIS FLOWER (UNII: W5BET37294) (PRIMULA VERIS FLOWER - UNII:W5BET37294)	PRIMULA VERIS FLOWER	1 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-7210-3	60 mL in 1 BOTTLE, DROPPER; 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(48951-7210)