Argentum Quartz

ARGENTUM QUARTZ- argentum quartz 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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Argentum Quartz

Directions: FOR ORAL USE.

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

Active Ingredients: Argentum met. (Silver) 20X, Quartz (Rock crystal) 30X

Inactive Ingredients: Water, Salt

Use: Temporary relief of ear irritation.

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

ArgentumQuartzAmpule

ARGENTUM QUARTZ
argentum quartz liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-1098
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	20 [hp_X] in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	30 [hp_X] in 1 mL

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:48951-1098-1	10 in 1 BOX	09/01/2009
1		1 mL in 1 AMPULE; Type 0: Not a Combination Product

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

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-1098)