ARNICARE- arnica montana cream 
Laboratoires Boiron
Reference Label Set Id: 28b3d04b-936f-5c7c-e054-00144ff8d46c

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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Arnicare Cream

Arnica Montana 1X HPUS 7%*

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.

Arnicare Cream

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

Arnicare Cream (without disodium EDTA)

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)

or

Tube 4.2 OZ (120G)

or

Tube 0.5 OZ (14G)

Arnica Montana 1X ... Trauma, muscle pain and stiffness, swelling from injuries, discoloration from bruising.

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

Questions, Comments?

www.arnicare.com

www.boironusa.com

info@boironusa.com

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



Distributed by Boiron Inc.
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, mucous membranes, damaged skin or wounds.

Do not use if you are allergic to Arnica montana or any of the this product's inactive ingredients.

When using this product, use only as directed: do not tightly wrap or bandage, do not apply heat or ice to the treated area immediately before or after use.

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

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

ɨ Homeopathic mother tincture made from Arnica montana fresh whole plant.

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ARNICARE 
arnica montana cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-9021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA1 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
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)  
PEGOXOL 7 STEARATE (UNII: 3EW5AXE5X5)  
ALCOHOL (UNII: 3K9958V90M)  
HYDROGENATED PALM/PALM KERNEL OIL PEG-6 ESTERS (UNII: 8EPU9MJ01K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0220-9021-6040 g in 1 TUBE; Type 0: Not a Combination Product03/01/2007
2NDC:0220-9021-6370 g in 1 TUBE; Type 0: Not a Combination Product03/01/2007
3NDC:0220-9021-821 in 1 PACKAGE06/01/2018
3120 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:0220-9021-681 in 1 BOX02/29/2016
414 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic03/01/2007
Labeler - Laboratoires Boiron (282560473)
Registrant - Boiron Inc. (014892269)
Establishment
NameAddressID/FEIBusiness Operations
Boiron282560473manufacture(0220-9021)

Revised: 3/2023
Document Id: f60007c0-9b09-273c-e053-2995a90a77d9
Set id: 542b41dd-f285-4e48-a67b-8e69523b143a
Version: 17
Effective Time: 20230303
 
Laboratoires Boiron