Label: CLEARASIL DAILY CLEAR OIL-FREE DAILY FACE WASH- salicylic acid lotion

  • NDC Code(s): 63824-350-01, 63824-350-78
  • Packager: RB Health (US) LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 7, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug facts

  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne medication

  • Use

    for the treatment of acne

  • Warnings

    For external use only

    When using this product

    • avoid contact with the eyes. If product gets into the eyes rinse 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.
    • limit use to the face and neck

    Stop use and ask a doctor ifskin or eye irritation develops

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet face
    • dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area
    • cover the entire affected area with a thin layer and rinse thoroughly with warm water one to three times daily
    • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
    • if bothersome dryness occurs, reduce application to once a day or every other day
  • Other information

    • keep tightly closed
    • store in a cool, dry place
  • Inactive ingredients

    water, glycerin, myristic acid, stearic acid, sodium lauroyl sarcosinate, palmitic acid, potassium hydroxide, lauric acid, polyquaternium 10, fragrance, phenoxyethanol, tetrasodium EDTA, pentasodium pentetate, tetrasodium etidronate, menthol, methylparaben, butylparaben, ethylparaben, isobutylparaben, propylparaben, aloe barbadensis leaf juice, maltodextrin, potassium sorbate, sodium benzoate

  • Questions?

    Call 1-866-25-CLEAR (1-866-252-5327).
    You may also report side effects to this phone number.

  • SPL UNCLASSIFIED SECTION

    Distributed by: Reckitt Benckiser LLC
    Parsippany, NJ 07054-0224
    © 2012 RB

  • PRINCIPAL DISPLAY PANEL - 230 mL Tube Label

    +20% FREE
    vs. 6.5 FL OZ size

    Clearasil®

    DAILY CLEAR®

    Oil-Free
    Daily Face Wash
    Salicylic Acid 2% Acne Medication

    Up to
    85% fewer
    breakouts in
    just 4 weeks

    NON-DRYING

    7.8 FL OZ (230 mL)

    Principal Display Panel - 230 mL Tube Label
  • INGREDIENTS AND APPEARANCE
    CLEARASIL  DAILY CLEAR OIL-FREE DAILY FACE WASH
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-350
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)  
    ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-350-78230 mL in 1 TUBE; Type 0: Not a Combination Product06/24/201209/01/2024
    2NDC:63824-350-01184 mL in 1 TUBE; Type 0: Not a Combination Product06/24/201209/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/24/201209/01/2024
    Labeler - RB Health (US) LLC (081049410)