ARNICA 30- arncia 30 gel

Arnica 30 by

Drug Labeling and Warnings

Arnica 30 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 TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION

Apply to skin as needed. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: Arnica extract

INACTIVE INGREDIENT

Inactive Ingredients: Spring water, Glycerin, Boric acid, Sodium alginate, Lavender oil, Sodium hydroxide, Sorbic acid, Tea tree oil, Grapefruit seed extract

Prepared using rhythmical processes.

PURPOSE

Uses: Temporary relief of bruises, sprains and minor cuts.

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, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

QUESTIONS

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARNICA 30 
arncia 30 gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-1399
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ)	ARNICA MONTANA FLOWER	1 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CITRUS PARADISI SEED (UNII: 12F08874Y7)
LAVENDER OIL (UNII: ZBP1YXW0H8)
WATER (UNII: 059QF0KO0R)
BORIC ACID (UNII: R57ZHV85D4)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM ALGINATE (UNII: C269C4G2ZQ)
SORBIC ACID (UNII: X045WJ989B)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-1399-2	30 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009

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(48951-1399)