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Name:Arnicare
Manufacturer:Labratoires Boiron
Category:Homeopathic Marketed Drugs


Consumer Label

ARNICARE  - arnica montana gel 
Labratoires Boiron

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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Consumer Label

Arnica montana 1X

For relief of muscle pain and stiffness due to minor injuries, overexertion and falls. Reduces pain and swelling as well as discoloration from bruising.

Do not use if tube seal is broken.

Apply a thin layer of Arnicare Gel to the affected area as soon as possible after minor injury. Repeat 3 times a day or as needed.

Alcohol, carbomer, dimethicone copolyol, sodium hydroxide. purified water

Arnicare Gel Imagearnicare image

Tube 2.6 OZ

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

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

Questions, Comments?

www.boironusa.com

info@boironusa.com

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

Boiron Information Center
6 Campus Boulevard
Newtown Square, PA 19073-3267


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

Keep out of reach of children




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

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


ARNICARE 
arnica montana gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9000
Route of Administration CUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARNICA MONTANA (ARNICA MONTANA) ARNICA MONTANA 1 [hp_X]
Inactive Ingredients
Ingredient Name Strength
ALCOHOL  
DIMETHICONE  
WATER  
SODIUM HYDROXIDE  
CARBOMER HOMOPOLYMER TYPE C  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0220-9000-59 1 GEL ( TUBE) in 1 CARTON None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 01/09/2007

Labeler - Labratoires Boiron (282560473)
Registrant - Boiron Inc. (014892269)
Establishment
Name Address ID/FEI Operations
Labratoires Boiron 279527290 manufacture
Establishment
Name Address ID/FEI Operations
Labratoires Boiron 282560473 manufacture

Revised: 10/2010 Labratoires Boiron



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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