Label: PHISODERM CLEAR CONFIDENCE FACE SCRUB- salicylic acid gel

  • NDC Code(s): 10742-1233-1
  • 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 pimples

  • Warnings

    For external use only

    When using this product

    • keep away from 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
    • squeeze scrub into hands and massage gently over face and neck
    • rinse thoroughly and pat dry
  • Inactive ingredients

    acrylates copolymer, aloe barbadensis leaf juice, anhydrous citric acid, butylene glycol, cocamidopropyl betaine, diazolidinyl urea, edetate disodium, fragrance, glycerin, iron oxides, jojoba esters, methylparaben, microcrystalline wax, PEG-8/SMDI copolymer, portulaca oleracea extract, potassium C12-13 alkyl phosphate, propylene glycol, propylparaben, purified water, sodium C14-16 olefin sulfonate, trolamine, violet 2

  • Questions?

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

  • Package/Label Principal Display Panel

    pHisoderm Clear Confidence Face Scrub
  • INGREDIENTS AND APPEARANCE
    PHISODERM CLEAR CONFIDENCE FACE SCRUB 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-1233
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)  
    PURSLANE (UNII: M6S840WXG5)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-1233-1142 g in 1 TUBE; 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(10742-1233)