ARNICARE- arnica montana ointment

Arnicare by

Drug Labeling and Warnings

Arnicare by is a Homeopathic medication manufactured, distributed, or labeled by Laboratoires Boiron, Boiron Inc., Boiron. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Arnica montana 1X

INDICATIONS & USAGE

Temporarily relives muscle pain and stiffness due to minor injuries, overexertion and falls.

DO NOT USE

Do not use if glued carton en flaps are open or if the tube seal is broken

DOSAGE & ADMINISTRATION

Apply a thin layer of Arnicare Ointment to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed.

INACTIVE INGREDIENT

Alcohol, purified water, petrolatum USP

HOW SUPPLIED

1 oz tube

PURPOSE

Arnica montana 1X ...trauma, muscle pain and stiffness, swelling from injuries, discoloration from bruising.

STORAGE AND HANDLING

Store at 68-77 O F (20-25 O C)

QUESTIONS

Questions, Comments?

www.arnicare.com

www.boironusa.com

info@boironusa.com

1-800-BOIRON-1 (1-800-264-7661)

Distributed by Boiron Inc.
6 Campus Boulevard
Newtown Square, PA 19073-3267

ASK DOCTOR

STOP USE

Stop use and ask dotcor if condition persists for more than 3 days or worsens.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

PREGNANCY OR BREAST FEEDING

WHEN USING

DRUG INTERACTIONS

WARNINGS

For external use only
Avoid contact with eyes and with open wounds.

If swallowed, get medical help or contact a Poison Control Center immediately

PRINCIPAL DISPLAY PANEL

Arnicare Ointment Image

INGREDIENTS AND APPEARANCE

ARNICARE 
arnica montana ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0220-9023
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	1 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0220-9023-51	30 g in 1 BOX; Type 0: Not a Combination Product	06/02/2007

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/02/2007

Labeler - Laboratoires Boiron (282560473)

Registrant - Boiron Inc. (014892269)

Establishment
Name	Address	ID/FEI	Business Operations
Boiron		282560473	manufacture(0220-9023)