Label: EQUATE ONE-STEP MEDICATED CORN REMOVERS- salicylic acid patch

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

Drug Label Information

Updated December 12, 2023

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  • Drug Facts

  • Active ingredient

    Salicylic acid 40%

    Purpose

    Corn Remover

  • Use

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

    For external use only.

    Ask a doctor before use if you have

    • diabetes
    • poor blood circulation

    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: may soak corn in warm water for 5 minutes
    • dry area thoroughly
    • remove bandage strips by peeling backing off
    • adhere medicated patch directly over corn
    • repeat this procedure every 48 hours as needed (until corn is removed) for up to 14 days
  • Other information

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

  • Inactive ingredients

    lanolin, paraffin, petrolatum

  • Questions or comments?

    1-888-287-1915

  • Package Labeling:

    Outer LabelLabel2

  • INGREDIENTS AND APPEARANCE
    EQUATE ONE-STEP MEDICATED CORN REMOVERS 
    salicylic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-224
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-224-061 in 1 BOX10/12/2023
    16 in 1 POUCH
    1100 mg in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03010/12/2023
    Labeler - Walmart Inc. (051957769)
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