Label: CLN ACNE CLEANSER- salicylic acid 0.5% liquid liquid

  • NDC Code(s): 69530-857-46, 69530-857-47, 69530-857-48
  • Packager: TopMD Skin Care, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 2, 2025

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

  • Drug Facts

  • Active Ingredients

    Salicylic Acid 0.5%

  • Purpose

    Acne Treatment

  • Uses

    For the treatment of acne

  • 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.

    Avoid contact with eyes.

    If contact occurs, flush thoroughly with water

    Keep out of reach of children.

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

  • Directions

    Cleanse twice daily or as indicated by your physician. Treat whole area. Wet the skin. Dispense into wet hands. Massage area gently for 30 seconds working to create a lather. Rinse thoroughly with warm water. If bothersome dryness or peeling occurs, reduce use to once a day or every other day.

  • Inactive Ingredients

    Purified Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide MEA, PEG-120 Methyl Glucose Trioleate, Propanediol, Sodium Hypochlorite, Disodium EDTA, Sodium Hydroxide.

  • PRINCIPAL DISPLAY PANEL

    Label CLn Acne Cleaser 34 fl oz

  • INGREDIENTS AND APPEARANCE
    CLN ACNE CLEANSER 
    salicylic acid 0.5% liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69530-857
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69530-857-46100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2016
    2NDC:69530-857-4730 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2016
    3NDC:69530-857-48240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/01/2016
    Labeler - TopMD Skin Care, Inc. (060946293)