ARNICARE- arnica montana gel 
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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Arnicare Gel

Active ingredient**

Arnica montana 1X HPUS 7%

The letters HPUS indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

Purpose*

Arnica montana 1X HPUS 7% Relieves muscle pain & stiffness, swelling from injuries, discoloration from bruises

Uses*

temporarily relieves muscle pain and stiffness due to:

reduces symptoms of bruising such as:

Warnings

For external use only.

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

When using this product

avoid contact with eyes, mucous membranes, wounds, damaged or irritated skin

use only as directed

dryness or irritation may occur

do not tightly wrap or bandage the treated area

do not apply heat or ice to treated area immediately before or after use

Stop use and ask a doctor if

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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. If heat or ice is applied, wait 5 minutes before applying Arnicare Gel.

Arnicare Gel Roll-On (2019)- Shake well before each use. With the applicator facing down, lightly squeeze the tube then roll ball against skin to apply a thin layer of the product to affected area. Massage gently into skin 3 times a day or as needed. If heat or ice is applied, wait 5 minutes before applying Arnicare Roll-on.

Arnicare Gel Roll-On (2023)- Twist roller to the "ON" position and gently squeeze tube to apply a thin layer of product to affected area. Twist roller to the "OFF" position and continue massaging as needed. Repeat 3 times a day. If heat or ice is applied, wait 5 minutes before applying Arnicare Roll-on Gel.

Alcohol, carbomer, purified water, sodium hydroxide

Other information

do not use if glued carton end flaps are open or if the tube seal is broken

do not use if pouch is torn or open

Arnicare Gel 0.18 oz (5g)- dispose 1 day after opening

Arnicare Gel Roll-On (2019)- dispose of 6 months after opening

Arnicare Gel Roll-On (2023)- dispose of 1 year after opening

0.18 oz (5g)

0.5 oz (14g)

1.5 oz (45g)

2.6 oz (75g)

4.2 oz (120g)

3 oz (90g)

Pain Relief*

Muscle Pain & Stiffness Swelling from Injuries Bruises*

*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.

Questions, Comments?

Distributed by Boiron, Inc., Newtown Square, PA 19073

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

BoironUSA.com

Arnicare.com

Info@Boiron.com

Made in France

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ARNICARE 
arnica montana gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-9000
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
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0220-9000-661 in 1 PACKAGE01/09/2007
1120 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0220-9000-591 in 1 PACKAGE01/09/2007
275 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:0220-9000-541 in 1 PACKAGE01/09/2007
345 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:0220-9000-651 in 1 PACKAGE01/09/2007
414 g in 1 TUBE; Type 0: Not a Combination Product
5NDC:0220-9000-841 in 1 PACKAGE06/01/2018
545 g in 1 TUBE; Type 0: Not a Combination Product
6NDC:0220-9000-862 in 1 PACKAGE06/01/2018
645 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:0220-9000-945 g in 1 POUCH; Type 0: Not a Combination Product06/09/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/09/2007
Labeler - Laboratoires Boiron (282560473)
Registrant - Boiron Inc. (014892269)
Establishment
NameAddressID/FEIBusiness Operations
Boiron282560473manufacture(0220-9000)

Revised: 6/2023
Document Id: ff599824-85fe-0ed5-e053-6294a90a1c87
Set id: ce519152-e6fb-42e3-8fd4-f819476ebd86
Version: 23
Effective Time: 20230630
 
Laboratoires Boiron