MANDRAGORA ARNICA liquid

Mandragora Arnica by

Drug Labeling and Warnings

Mandragora Arnica 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.

DOSAGE & ADMINISTRATION

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

ACTIVE INGREDIENT

Active Ingredients: Betula (Silver birch leaves) 3X, Mandragora (Mandrake) 3X, Meniscus genus (Bovine medial meniscus of the knee joint) 6X, Formica (Red wood ant) 10X, Arnica 15X, Equisetum (Common horsetail) 15X

INACTIVE INGREDIENT

Inactive Ingredients: Water, Salt

PURPOSE

Use: Temporary relief of sore joints.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: 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

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MANDRAGORA ARNICA 
mandragora arnica liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-7012
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO) (BETULA PUBESCENS LEAF - UNII:84SOH0O3OO)	BETULA PUBESCENS LEAF	3 [hp_X]  in 1 mL
MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB)	MANDRAGORA OFFICINARUM ROOT	3 [hp_X]  in 1 mL
SUS SCROFA MENISCUS (UNII: 1C8T78BD9Q) (SUS SCROFA MENISCUS - UNII:1C8T78BD9Q)	SUS SCROFA MENISCUS	6 [hp_X]  in 1 mL
FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5)	FORMICA RUFA	10 [hp_X]  in 1 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	15 [hp_X]  in 1 mL
EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z)	EQUISETUM ARVENSE TOP	15 [hp_X]  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-7012-1	10 in 1 BOX	09/01/2009
1		1 mL in 1 AMPULE; Type 0: Not a Combination Product

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(48951-7012)