Label: SALICYLIC ACID- gel callus remover patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 22, 2024

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  • 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

  • INGREDIENTS AND APPEARANCE
    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 DrugM03007/31/2018
    Labeler - CVS Pharmacy (062312574)
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