Eupatorium comp.

EUPATORIUM COMP.- eupatorium comp. 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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Eupatorium comp.

Directions: FOR ORAL USE.

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

Active Ingredients: Eupatorium (Hemp agrimony) 5X, Aconitum (Monkshood) 6X, Bryonia (White bryony) 6X, Phosphorus (Yellow phosphorus) 7X,
Lachesis (Bushmaster venom) 12X

Inactive Ingredients: Water, Salt

Use: Temporary relief of flu 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. 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

EupatoriumCompAmpules

EUPATORIUM COMP.
eupatorium comp. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-4049
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E)	EUPATORIUM PERFOLIATUM FLOWERING TOP	5 [hp_X] in 1 mL
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	6 [hp_X] in 1 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	6 [hp_X] in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	7 [hp_X] in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [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:48951-4049-1	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(48951-4049)