Label: PHISODERM CLEAR CONFIDENCE DAILY GEL FACE WASH- salicylic acid liquid

  • NDC Code(s): 10742-1412-1
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    treats and helps prevent acne blemishes

  • Warnings

    For external use only

    When using this product

    • avoid contact with the eyes. If contact occurs, flush thoroughly with water.
    • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

    If pregnant or breast-feeding

    ask a health professional before use.

  • Keep out of reach of children

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

  • Directions

    • wet face, then gently massage onto skin
    • rinse well and pat dry
    • use twice daily
  • Inactive ingredients

    water, sodium C14-16 olefin sulfonate, lauramidopropyl betaine, lauryl glucoside, sodium chloride, disodium EDTA, DMDM hydantoin, fragrance, iodopropynyl butylcarbamate, lactic acid, polysorbate 20, triethanolamine

  • Questions?

    Toll free 1-877-636-2677 MON-FRI 9 AM-5 PM (EST)

  • Principal Display Panel

    Phisoderm Clear Confidence Daily Gel Face Wash
  • Principal Display Panel

    Drug Facts
  • INGREDIENTS AND APPEARANCE
    PHISODERM CLEAR CONFIDENCE DAILY GEL FACE WASH 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-1412
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-1412-1177 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00605/01/2012
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-1412)
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