Echinacea Quartz Liquid [Uriel Pharmacy Inc.] -

ECHINACEA QUARTZ LIQUID [URIEL PHARMACY INC.]
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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 2: Consult a doctor.
ACTIVE INGREDIENT

Active Ingredients: Echinacea (Purple coneflower) 3X, Antimonite (Nat. antimony trisulfide) 6X, Argentum nitricum (Silver nitrate) 20X, Atropa belladonna (Nightshade) 20X, Quartz (Rock crystal) 20X
INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, Organic cane alcohol, Rose oil, Lactose
PURPOSE

Uses: Temporarily relieves pain of sensitive teeth, soreness in mouth or gum inflammation.
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. Contains traces of lactose. 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

ECHINACEA QUARTZ
echinacea quartz liquid

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX)	ECHINACEA, UNSPECIFIED	3 [hp_X] in 1 mL
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	6 [hp_X] in 1 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	20 [hp_X] in 1 mL
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H)	ATROPA BELLADONNA	20 [hp_X] in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	20 [hp_X] in 1 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-4131-3	60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/01/2009

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(48951-4131)

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