Label: MEDICATED CORN REMOVER- salicylic acid patch

  • NDC Code(s): 55910-857-01
  • Packager: Dolgencorp, Inc. (Dollar General & Rexall)
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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  • Active ingredient

    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 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 thoroughly
    • if necessary, cut medicated patch to fit corn
    • carefully adhere medicated patch directly over 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° to 30°C (59° and 86°F)

  • Inactive ingredients

    acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

  • ​Questions?

    call 1-866-4-REXALL

  • ​Principal Display Panel

    Rexall Pharmacy

    MEDICATED

    CORN REMOVERS
    Salicylic Acid 40%

    Effective corn removal treartment

    Cushioning pads help protect against pressure & friction

    9 MEDICATED PATCHES/ 9 Pads Image 1

  • INGREDIENTS AND APPEARANCE
    MEDICATED CORN REMOVER 
    salicylic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-857
    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:55910-857-019 in 1 PACKAGE; Type 0: Not a Combination Product11/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03011/01/2015
    Labeler - Dolgencorp, Inc. (Dollar General & Rexall) (068331990)
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