ARNICA MONTANA- arnica montana gel 
WALGREENS CO.

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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Walgreens Arnica Pain Relieving Gel
Arnica Montana1X HPUS 7%

Arnica montana 1X HPUS 7%

alcohol, carbomer, purified water, sodium hydroxide

Apply a thin layer of gel to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed.

temporarily relieves muscle pain and stiffness due to minor injuries, overexertion and falls, reduces pain, swelling and discoloration from bruises

For external use only

When using this product avoid contact with eyes, mucous membranes, damaged skin, or wounds.

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

When using this product use only as directed, do not bandage tightly or use a heating pad.

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

Keep out of reach of children.

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

Keep out of reach of children.

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

Trauma, muscle pain, and stiffness, swelling from injuries, discoloration from bruising

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

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

CT515026LB515026

ARNICA MONTANA 
arnica montana gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5150
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 940 (UNII: 4Q93RCW27E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-5150-2674 g in 1 PACKAGE; Type 0: Not a Combination Product06/20/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/20/2019
Labeler - WALGREENS CO. (008965063)

Revised: 4/2022
Document Id: dc793108-68db-1323-e053-2995a90af598
Set id: 995d7e44-83a4-0d31-e053-2a95a90a2acb
Version: 4
Effective Time: 20220412
 
WALGREENS CO.