Label: SCOTT CLEAR CORN REMOVERS- 40% w/w salicylic acid corn remover plaster

  • NDC Code(s): 82660-006-05
  • Packager: Creative Foam Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 12, 2024

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  • Active Ingredient

    Salicylic Acid 40% w/w

  • Purpose

    Corn Removal

  • Uses

    • For removal of corns
    • Relieves pain by removing corns
  • Warning

    For external use only

  • Do not use:

    • If you are a diabetic
    • If you have poor blood circulation
    • On irritated skin or area that is infected or reddened
  • STOP USE

    Stop use and ask a doctor if discomfort lasts

  • Keep out of reach of children

  • Keep out of reach of children

    If swallowed get medical help or contact a Poison Control Center immediately.

  • Directions:

    Wash affected area, dry thoroughly
    If necessary, cut medicated disk to fit corn
    Apply medicated disk with sitcky side adhereing to skin
    Cover medicated disk with enclosed cushion
    After 48 hours, remove disk
    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 a

  • Other Information

    Store between 15 o C and 30 o C (59 o F and 86 o F)

  • Inactive Ingredients

    Vinyl Acetate

  • Scott Clear Corn Removers

    Scott Clear Corn Removers

  • INGREDIENTS AND APPEARANCE
    SCOTT CLEAR CORN REMOVERS 
    40% w/w salicylic acid corn remover plaster
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82660-006
    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, UNSPECIFIED (UNII: 532B59J990)  
    ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82660-006-05100 mg in 1 BOX; Type 0: Not a Combination Product12/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03012/31/2020
    Labeler - Creative Foam Corporation (620897061)
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