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
  • 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 17, 2023

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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 finalpart358F11/01/2015
    Labeler - Dolgencorp, Inc. (Dollar General & Rexall) (068331990)
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