Label: VERACITI- salicylic acid gel

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

Drug Label Information

Updated January 8, 2026

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  • Active ingredient

    Salicylic acid 17% w/w

  • Purpose

    Wart Remover

  • Uses

    • 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.

    Do not use

    on irritated, infected or reddened skin, moles, birthmarks, warts with hair growing from them, warts on the face, genitals or mucous membranes.

    Ask a doctor before use if

    you are diabetic or have poor circulation.

    When using this product

    avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes. Avoid inhaling vapors.

    Stop use and ask a doctor if

    discomfort persists.

    Extremely flammable.

    Keep away from fire and flame. Cap tube tightly and store at room temperature away from heat.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Wash affected area. May soak wart in warm, not hot, water for 5 minutes. Dry affected area thoroughly. Apply one drop at a time to suffciently cover each wart. Let completely dry. Repeat procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.

  • Inactive ingredients

    Flexible Collodion, Glycolic Acid, Hydroxypropylcellulose, Isopropyl Alcohol, Malic Acid, SD 40 Alcohol (43.5%)

  • Questions or Suggestions?

    1.855.763.8733 or visit us at www.thepodiatreecompany.com. Our commitment to you is 100% satisfaction. If you are not

    completely satisfied, please contact us directly for a full refund.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    VERACITI 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54633-115
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID17 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PYROXYLIN (UNII: KYR8BR2X6O)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    MALIC ACID (UNII: 817L1N4CKP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54633-115-1515 g in 1 TUBE; Type 0: Not a Combination Product10/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02810/01/2015
    Labeler - The Podiatree Company (078656000)
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