Label: SALICYLIC ACID- medicated corn removers patch

  • NDC Code(s): 70000-0330-1
  • Packager: LEADER/ Cardinal Health 110, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 21, 2024

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  • ​Active ingredient

    Salicylic acid 40%

  • Purpose

    Callus remover

  • Use

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

    For external use only.

    Do not use

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

    If discomfort persists see your doctor or podiatrist

    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
    • if necessary, cut medicated patch to fit corn
    • apply adhesive side down of medicated patch onto corn
    • cover medicated patch with pad
    • after 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 15 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

    ​LEADER

    Medicated Corn Removers

    Salicylic Acid 40% | Corn Remover

    • ​Effective Corn Removal Treatment
    • Cushions Against Pressure and Friction

    9 Medicated Patches/9 Protective Pads

    Corn Remover

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    medicated corn removers patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0330
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID400 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    VINYL ACETATE (UNII: L9MK238N77)  
    POLYVINYL ALCOHOL (UNII: 532B59J990)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70000-0330-19 in 1 CARTON02/21/2018
    11 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03002/21/2018
    Labeler - LEADER/ Cardinal Health 110, Inc. (063997360)
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