SALICYLIC ACID- gel callus remover patch 
CVS Pharmacy

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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CVS Gel Callus Remover

Active Ingredient

Salicylic acid 40%

Purpose

Callus Remover

Uses

  • for the removal of calluses
  • releves pain by removing calluses

Warnings

For external use only.

Do not use

  • if you are a diabetic
  • have poor blood circulation
  • on irritated skin, on any area that is infected or reddened

Stop use and ask doctor

if discomfort persists.

Keep out of reach of children.

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

Directions

  • wash affected area and dry thoroughly
  • apply adhesive side down of medicated disc on to the callus
  • cover the medicated disc with gel cushion
  • after 48 hours, remove medicated disc
  • repeat this procedure every 48 hours as needed for up to 14 days (until callus is removed)
  • may soak callus in warm water for 5 minutes to assist in removal

Other information

store between 15°C to 30°C (59°F to 86°F)

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

call 1-866-964-0939

Principal Display Panel

CVS Health

Medicated

Gel Callus Removers

SALICYLIC ACID 40%

  • Maximum strength salicylic acid removes calluses safely & effectively
  • Cushions & conceals
  • Thin & flexible to fit inside shoes

4 CUSHIONS

4 MEDICATED DISCS

gel callus removers

SALICYLIC ACID 
gel callus remover patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-202
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 4 
Inactive Ingredients
Ingredient NameStrength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
VINYL ACETATE (UNII: L9MK238N77)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-202-044 in 1 PACKAGE; Type 0: Not a Combination Product07/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F07/31/2018
Labeler - CVS Pharmacy (062312574)

Revised: 7/2021
Document Id: c743356e-6991-0c03-e053-2a95a90a4e07
Set id: 075328fb-297b-459f-adad-d50847fea965
Version: 4
Effective Time: 20210716
 
CVS Pharmacy