Label: SALICYLIC ACID- medicated callus removers extra thick patch

  • NDC Code(s): 41163-135-04
  • Packager: United Natural Foods, Inc. dba UNFI
  • 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

    Callus remover

  • Use

    • for the removal of calluses
    • relieves pain by removing calluses
  • 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

    ​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 callus
    • apply adhesive side down of medicated patch onto callus
    • 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°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

    Equaline

    extra thick

    callus removers
    pads
    salicylic acid

    • effective and safe removal of calluses
    • protects against pressure & pain

    4 PADS

    4 MEDICATED PATCHES

    Equaline_Callus Removers Extra Thick_52-072EQ.jpg

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    medicated callus removers extra thick patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-135
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 4 
    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:41163-135-044 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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