ARNICARE PROCEDURE RECOVERY- arnica montana 
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 Procedure Recovery Kit

Active ingredient** (in each pellet)

Arnica montana 12C (0.443 mg)

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

Purpose*

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:

Stop use and ask a doctor if symptoms persist for more than 3 days or get worse, new symptoms occur, or redness or swelling is present. These could be signs of a serious condition.

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Directions

Before procedure: Dissolve 5 pellets under the tongue 3 times a day for 2 days.

After procedure: Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved.

lactose, sucrose

Questions, Comments?
www.boironusa.com
info@boironusa.com

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

Newtown Square, PA 19073-3267

do not use if pellet dispenser seal is broken

3 tubes of Boiron Arnica montana 12C** HPUS

Provides approximately 15 days of treatment

Made in France

Boiron Arnica montana pellets reduce bruising, swelling, and pain used before and after your procedure.

Non-habit forming

Non-drowsy

No known drug interactions

post-operative care*

Dissolve 5 pellets under the tongue 3 times a day for 2 days.

Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved.

Turn tube upside down. Twist until 5 pellets are dispensed. Remove cap and pour pellets under the tongue.

*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.

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ARNICARE PROCEDURE RECOVERY 
arnica montana kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-9050
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0220-9050-751 in 1 PACKAGE11/01/2007
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 10 TUBE
Part 1 of 1
ARNICA 
arnica montana pellet
Product Information
Item Code (Source)NDC:0220-0508
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA30 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE (UNII: J2B2A4N98G)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUND (Pellet) Size4mm
FlavorImprint Code ;
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0220-0508-4180 in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic11/01/2007
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic11/01/2007
Labeler - Laboratoires Boiron (282560473)
Registrant - Boiron Inc. (014892269)
Establishment
NameAddressID/FEIBusiness Operations
Boiron282560473manufacture(0220-9050)

Revised: 1/2023
Document Id: f1875a4f-fc44-cb91-e053-2995a90addeb
Set id: f0003627-b81c-46b6-8773-4f2987b75739
Version: 7
Effective Time: 20230105
 
Laboratoires Boiron