Label: EXTRA THICK CALLUS REMOVERS- extra thick callus removers with salicylic acid patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 25, 2023

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  • Active ingredient

    Salicylic acid 40%

  • Purpose

    Callus remover

  • ​Uses

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

    For external use only.

    ​Do not use

    • if you are 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 patches to fit callus
    • apply the 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 callus is removed)
    • may soak callus in warm water for 5 minutes to assist in removal
  • ​Other information

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

  • ​Inactive ingredients

    acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

  • ​Questions?

    call 1-888-287-1915

  • Principal Display Panel

    Equate

    Extra Thick Callus Removers


    Salicylic Acid 40%

    • Effective callus removal treatment
    • Extra thick pads protect against friction and reduce pressure

    4 Medicated Patches/ 4 Pads

    Extra Thick Callus Remover

  • INGREDIENTS AND APPEARANCE
    EXTRA THICK CALLUS REMOVERS 
    extra thick callus removers with salicylic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-019
    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
    POLYVINYL ALCOHOL (UNII: 532B59J990)  
    VINYL ACETATE (UNII: L9MK238N77)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-019-04160 mg in 1 PACKAGE; Type 0: Not a Combination Product08/01/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358F08/01/2013
    Labeler - Wal-Mart Stores, Inc. (051957769)
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