Label: SKINCEUTICALS CLARIFYING EXFOLIATING CLEANSER- salicylic acid cream

  • NDC Code(s): 49967-468-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 28, 2023

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  • Active ingredient


    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    • for the treatment of acne
    • reduces the number of acne blemishes, blackheads, and whiteheads and allows skin to heal
  • Warnings

    For external use only

  • When using this product

    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.

  • Keep out of reach of children.

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

  • Directions

    • use once daily
    • wet face
    • squeeze small amount of cleanser and work into hands
    • apply to face and massage gently
    • rinse thoroughly
    • if bothersome drying or peeling occurs, reduce application to every other day
  • Inactive ingredients

    water, propylene glycol, behenyl betaine, triethanolamine, glycolic acid, lactic acid, pumice, sodium chloride, phenoxyethanol, PEG-100 sterarate, zinc PCA, glyceryl stearate, disodium EDTA, sodium benzoate

  • Questions?

    Call 800-811-1660

    Monday - Friday (9 a.m. - 5 p.m. CST)

  • PRINCIPAL DISPLAY PANEL

    image of a label

    image of a label
  • INGREDIENTS AND APPEARANCE
    SKINCEUTICALS CLARIFYING EXFOLIATING CLEANSER 
    salicylic acid cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-468
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BEHENYL BETAINE (UNII: 385A69N40W)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    PUMICE (UNII: NT5NN5KL16)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-10 STEARATE (UNII: D3AHD468TV)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-468-01150 mL in 1 TUBE; Type 0: Not a Combination Product01/27/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00601/27/2017
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmetic Essence, LLC032565959manufacture(49967-468)
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