Label: EQUATE ONE STEP WART REMOVER STRIPS- salicylic acid plaster

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • Drug Facts

  • Active ingredient

    Salicylic acid 40%

    Purpose

    Wart Remover

  • Uses

    • for the removal of common and plantar warts
    • the common wart is easily recognized by the rough “cauliflower-like” appearance of the surface
    • the plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the footprint pattern
  • Warnings

    For external use only.

    Do not use

    • on irritated skin or on any area that is infected or reddened
    • on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes
    • if you have diabetes or poor blood circulation

    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 (1-800-222-1222) right away.

  • Directions

    • wash affected area: may soak wart in warm water for 5 minutes
    • dry area thoroughly
    • peel off backing paper
    • adhere medicated patch directly over wart
    • repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
  • Other information

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

  • Inactive ingredients

    lanolin, paraffin, petrolatum.

  • Questions or comments?

    1-888-287-1915

  • Package Labeling:

    LabelInner label

  • INGREDIENTS AND APPEARANCE
    EQUATE ONE STEP WART REMOVER STRIPS 
    salicylic acid plaster
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-226
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-226-011 in 1 BOX10/12/2023
    114 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02810/12/2023
    Labeler - Walmart Inc. (051957769)
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