Cinnabar Dandelion

CINNABAR DANDELION- cinnabar dandelion 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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Cinnabar Dandelion

Directions: FOR ORAL USE.

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

Active Ingredients: Agropyron (Couch grass) 3X, Taraxacum (Dandelion) 3X, Pyrite (Nat. Iron disulfide) 8X, Kali carb e cinere Fagi (Potassium carbonate from beech wood ash) 10X, Cinnabaris (Nat. mercuric sulfide) 20X

Inactive Ingredients: Water, Salt, Lactose

Uses: Temporary relief of cold, flu and sore throat symptoms.

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. Contains traces of lactose. 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 shopuriel.com Lot:

Cinnabar Dandelion Ampules

CINNABAR DANDELION
cinnabar dandelion liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-3101
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (ELYMUS REPENS ROOT - UNII:3IXW0F6P8W)	ELYMUS REPENS ROOT	3 [hp_X] in 1 mL
TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (TARAXACUM PALUSTRE ROOT - UNII:GCZ4W7077C)	TARAXACUM PALUSTRE ROOT	3 [hp_X] in 1 mL
FERROUS DISULFIDE (UNII: 132N09W4PR) (FERROUS CATION - UNII:GW89581OWR)	FERROUS DISULFIDE	8 [hp_X] in 1 mL
CARBONATE ION (UNII: 7UJQ5OPE7D) (CARBONATE ION - UNII:7UJQ5OPE7D)	CARBONATE ION	10 [hp_X] in 1 mL
MERCURIC CATION (UNII: ED30FJ8Y42) (MERCURIC CATION - UNII:ED30FJ8Y42)	MERCURIC CATION	20 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LACTOSE (UNII: J2B2A4N98G)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:48951-3101-1	10 in 1 BOX	09/01/2009
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

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-3101)