Label: SALICYLIC ACID- medicated corn removers patch

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

Drug Label Information

Updated December 16, 2024

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  • Active Ingredients

    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
    • if you 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
    • if necessary, cut medicated patch to fit corn
    • apply adhesive side 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 5 minutes to assist in removal
  • Other Information

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

  • Inactive Ingredients

    acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

  • Questions?

    1-888-287-1915

  • Principal Display Panel

    equate

    Medicated

    Corn

    Removers

    Salicylic Acid 40%

    • Effective corn removal treatment
    • Cushions against pressure & friction

    9 Medicated Patches/9 Pads

    Equate Corn Remover 9 CT

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    medicated corn removers patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-155
    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
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-155-099 in 1 PACKAGE; Type 0: Not a Combination Product03/15/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03003/15/2019
    Labeler - Wal-Mart Stores Inc (051957769)
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