ARNICARE - arnica montana cream 
Laboratoires 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

Temporarily relieves muscle pain and stiffness due to minor injuries, overexertion and falls. Reduces pain, swelling and discoloration from bruises.

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

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

Alcohol, Caprylyl glycol, carbomer, cetyl palmitate, EDTA disodium, glycerin, lauroyl macrogolglycerides, pegoxol-7 stearate, purified water, sodium hydroxide, sorbic acid, 1,2-hexanediol

Tube 2.5 OZ (70 G)
or
Tube 1.33 OZ (40G)

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.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


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

Keep out of reach of children



Unscented - Paraben-Free - Great for massage - Works naturally with your body

For external use only
Avoid contact with eyes.

If swallowed, get medical help or contact a Poison Control Center right away.

Arnicare cream image

ARNICARE 
arnica montana cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9021
Route of Administration TOPICAL DEA Schedule     
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
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CARBOMER 934 (UNII: Z135WT9208)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SORBIC ACID (UNII: X045WJ989B)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)  
PEGOXOL 7 STEARATE (UNII: 3EW5AXE5X5)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0220-9021-60 40 g in 1 TUBE
2 NDC:0220-9021-63 70 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 03/15/2007
Labeler - Laboratoires Boiron (282560473)
Registrant - Boiron Inc. (014892269)

Revised: 3/2015
Document Id: 7f7f8963-af82-4ab0-98c1-d417d8bf9d7c
Set id: 542b41dd-f285-4e48-a67b-8e69523b143a
Version: 7
Effective Time: 20150301
 
Laboratoires Boiron