ARNICARE ARNICA- arnica montana tablet

Arnicare Arnica by

Drug Labeling and Warnings

Arnicare Arnica 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 9C

INDICATIONS & USAGE

Temporary relieves muscle pain and stiffness due to minor injuries, overexertion and falls.

Reduces pain, swelling and discoloration from bruises.

INACTIVE INGREDIENT

Croscarmellose sodium, lactose, magnesium, stearate.

HOW SUPPLIED

60 tablets

PURPOSE

Arnica Montana 9C 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.boironusa.com
info@boironusa.com 1-800-BOIRON-1
(1-800-264-7661)
Boiron Information Center
6 campus Bouelvard
Newtown Square, PA
19073-3267

ASK DOCTOR

STOP USE

Stop use and ask a doctor if symptoms persist continuously for more than 7 days or worsen, if new symptoms occur, or if redness or swelling is present because these could be signs of a serious illness.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

WHEN USING

DRUG INTERACTIONS

Non drowsy, no side effects, no drug interactions, works naturally with your body

WARNINGS

Do not use if glued carton end flaps or if the blister seal is broken.

DOSAGE & ADMINISTRATION

Adults and children 6 years of age and older: At the onset of symptoms dissolve 2 tablets in the mouth and repeat every hour for 2 more hours. Then, dissolve 2 tablets in the mouth every 6 hours until symptoms are relieved.

Children 2 to 6 years of age: Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above.

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before us.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARNICARE ARNICA 
arnica montana tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0220-9059
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	9 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND (BOIRON)	Size	9mm
Flavor		Imprint Code	;
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0220-9059-04	60 in 1 BLISTER PACK; Type 0: Not a Combination Product	07/11/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/11/2011

Labeler - Laboratoires Boiron (282560473)

Registrant - Boiron Inc. (014892269)

Establishment
Name	Address	ID/FEI	Business Operations
Boiron		282560473	manufacture(0220-9059)