Label: SALICYLIC ACID- medicated corn removers patch

  • NDC Code(s): 41163-136-09
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2024

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  • ​Active ingredient

    Salicylic acid 40%

  • Purpose

    Corn remover

  • Use

    • for the removal of 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, on 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 area thoroughly
    • if necessary, cut medicated patch to fit corn
    • apply adhesive side down of medicated patch onto corn
    • cover medicated patch with cover
    • 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°C to 30°C (59°F to 86°F)

  • ​Inactive ingredients

    acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

  • Questions?

    1-866-964-0939

  • Principal Display Panel

    Equaline

    medicated
    ultra thin
    corn remover

    pads

    salicylic acid

    • therapeutic corn removal treatment
    • ultra thin cushion helps relieve painful shoe pressure and friction
    • specifically designed for tight shoes

    9 Medicated Patches/ 9 Pads

    Equaline_Corn Removers Ultra Thin_52-056EQ.jpg

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    medicated corn removers patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-136
    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 (UNII: 532B59J990)  
    VINYL ACETATE (UNII: L9MK238N77)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-136-099 in 1 PACKAGE; Type 0: Not a Combination Product12/27/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03012/27/2017
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
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