Label: COMPOUND W- salicylic acid gel

  • NDC Code(s): 63029-595-12, 63029-595-14, 63029-595-25
  • Packager: Medtech Products Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 2, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • SPL UNCLASSIFIED SECTION

    Compound W®
    Salicylic Acid Wart Remover

    MAXIMUM STRENGTH
    FAST ACTING GEL

    NET WT 0.25 OZ (7 g)

    Drug Facts

  • Active ingredient

    Salicylic acid 17% w/w

  • Purpose

    Wart remover

  • Use

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

    For external use only.

    Flammable. Keep away from fire and flame.

    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

    When using this product

    • avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes.
    • avoid inhaling vapors
    • cap tightly and store at room temperature away from heat

    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
    • by squeezing tube gently, apply one drop at a time to sufficiently cover each wart
    • let dry
    • repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks
  • Other Information

    • store at room temperature
    • avoid excessive heat 37°C (99°F)
    • skin discoloration may occur during or after use
    • wipe the tip of the tube with a paper towel between uses
  • Inactive ingredients

    alcohol, camphor, castor oil, ethyl acetate, hydroxypropyl cellulose, hypophosphorous acid, isopropanol, nitrocellulose, polysorbate 80, water

  • Questions?

    1-800-443-4908 CompoundW.com

  • PRINCIPAL DISPLAY PANEL

    Compound W
    WART REMOVER SYSTEM
    MAXIMUM STRENGTH
    FAST ACTING GEL + CONSEAL
    Salicylic acid
    NET WT 0.25 OZ (7g)

    PRINCIPAL DISPLAY PANEL 
Compound W
WART REMOVER SYSTEM
MAXIMUM STRENGTH
FAST ACTING GEL + CONSEAL
Salicylic acid 
NET WT 0.25 OZ (7g)

  • PRINCIPAL DISPLAY PANEL

    Compound W
    Total Care Wart & Skin
    Salicylic acid – Wart Remover
    GEL NET WT 0.25 OZ (7g)

    Compound W
Total Care Wart & Skin 
Salicylic acid – Wart Remover 
GEL NET WT 0.25 OZ (7g)

  • PRINCIPAL DISPLAY PANEL

    Compound W
    Wart Remover
    Salicylic acid
    MAXIMUM STRENGTH
    GEL
    NET WT 0.25 OZ (7g)

    Compound W
Wart Remover
Salicylic acid
MAXIMUM STRENGTH
FAST ACTING GEL
NET WT 0.25 OZ (7g)

  • INGREDIENTS AND APPEARANCE
    COMPOUND W 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-595
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID170 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    ETHYL ACETATE (UNII: 76845O8NMZ)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PYROXYLIN (UNII: KYR8BR2X6O)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63029-595-251 in 1 CARTON03/15/2014
    17 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:63029-595-121 in 1 CARTON03/15/2014
    27 g in 1 TUBE; Type 1: Convenience Kit of Co-Package
    3NDC:63029-595-141 in 1 CARTON03/15/2014
    37 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02803/15/2014
    Labeler - Medtech Products Inc. (122715688)