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
  • 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 February 7, 2023

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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 finalpart333D05/01/2012
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-1412)
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