Label: CLEAR AWAY WART REMOVERS- salicylic acid disc

  • NDC Code(s): 73469-6421-2
  • Packager: Scholls Wellness Company LLC
  • 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 May 26, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredient

    Salicylic acid 40%

  • PURPOSE

    Purpose

    Wart Remover

  • INDICATIONS & USAGE

    for the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance on the surface.

  • WARNINGS

    For external use only

  • DO NOT USE

    • if you are a diabetic
    • if you have poor blood circulation
    • on irritated skin or any aea that is infected or reddened
    • on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes
  • ASK DOCTOR

    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 right away

  • DOSAGE & ADMINISTRATION

    • wash affected area
    • may soak wart in warm water for 5 minutes
    • dry area thoroughly
    • if necessary, cut medicated disc to fit wart
    • apply medicated disc with dark sticky side adhering to skin
    • covr medicated dosc with enclosed cushion
    • repeat procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
  • STORAGE AND HANDLING

    • store between 20° to 25°C (68° to 77°F)
    • protect from excessive heat and temperatures above 40°C (140°F)
  • INACTIVE INGREDIENT

    Inactive ingredients

    Antioxidant (CAS 991-84-4), iron oxides, mineral oil, petroleum hydrocarbon resin, silicon dioxide, synthetic polyisoprene rubber, talc

  • QUESTIONS

    Questions?

    1-866-360-3226

  • PRINCIPAL DISPLAY PANEL

    Clear Away Wart Removers

  • INGREDIENTS AND APPEARANCE
    CLEAR AWAY WART REMOVERS 
    salicylic acid disc
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73469-6421
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.4 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BROWN IRON OXIDE (UNII: 1N032N7MFO)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ANTIOXIDANT GS (UNII: 2BBL73FIEU)  
    TALC (UNII: 7SEV7J4R1U)  
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73469-6421-212 in 1 CARTON11/01/2019
    11 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02811/01/2019
    Labeler - Scholls Wellness Company LLC (117174744)
    Registrant - Scapa Tapes North America LLC (079995435)
    Establishment
    NameAddressID/FEIBusiness Operations
    Scapa Tapes North America Inc.079995435manufacture(73469-6421)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!