Label: SALICYLIC ACID- medicated corn remover patch

  • NDC Code(s): 63868-040-09
  • Packager: Chain Drug Marketing Association
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • Active Ingredient

    Salicylic Acid 40%

  • Purpose

    Corn Remover

  • Uses

    • for the removal of corns
    • relieves pain by removing corns
  • Warnings

    For External Use Only

    Do not use

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

    Stop use and ask a 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 area thoroughly
    • if necessary, cut medicated patch to fit corn
    • apply adhesive side down of medicated patch onto corn
    • cover medicated patch with padafter 48 hours, remove medicated patch
    • repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
    • may soak corn 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

    QC

    QUALITY CHOICE

    Medicated

    Corn

    Removers

    Salicylic Acid 40%

    Effective Corn Removal Treatment

    Cushions Against Pressure & Friction

    9 Pads

    9 Medicated Patches

    Quality Choice_Corn Removers_52-003QC.jpg

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    medicated corn remover patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 9 
    Inactive Ingredients
    Ingredient NameStrength
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    VINYL ACETATE (UNII: L9MK238N77)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-040-099 in 1 PACKAGE; Type 0: Not a Combination Product12/18/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03012/18/2017
    Labeler - Chain Drug Marketing Association (011920774)
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