Label: CLEAN AND CLEAR ADVANTAGE ACNE SPOT TREATMENT- salicylic acid lotion

  • NDC Code(s): 69968-0126-1
  • Packager: Johnson & Johnson Consumer Inc.
  • 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 January 5, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Salicylic Acid (2%)

  • Purpose

    Acne Medication

  • Use

    • For the treatment of acne
  • Warnings

    For external use only.

    Flammable, keep away from open fire or flame.

    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.
    • If eye 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

    • clean the skin thoroughly before applying this product.
    • cover the entire affected area with a thin layer 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 or peeling occurs, reduce application to once a day or every other day
  • Other Information

    Store at room temperature.

    Sunburn Alert

    This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards.

  • Inactive Ingredients

    Alcohol Denat., Water, Hamamelis Virginiana (Witch Hazel) Water, Polyacrylamide, Glycerin, Cyclopentasiloxane, C13-14 Isoparaffin, C12-15 Alkyl Lactate, Alcohol, Phenoxyethanol, Cetyl Lactate, PPG-2 Isoceteth-20 Acetate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Laureth-7, Polysorbate 20, Phenethyl Dimethicone, Fragrance, Dehydroxanthan Gum, Propylene Glycol, Benzalkonium Chloride, Ammonia, Tetrasodium EDTA, Butylene Glycol, Capryloyl Glycine, Sarcosine, Cinnamomum, Zeylanicum Bark Extract, Cedrus Atlantica Bark Extract, Portulaca Oleracea Extract

  • Questions?

    Call toll‐free 1-877-754-6411 or 215-273-8755 (collect).www.cleanandclear.com

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    JOHNSON & JOHNSON CONSUMER INC.
    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 22 mL Tube Carton

    Clean

    &

    Clear ®

    advantage

    acne spot

    treatment

    salicylic acid acne medication

    OIL-FREE

    +WITCH HAZEL

    100% of people

    showed clearer skin

    in just one day

    won't overdry skin

    0.75 FL. OZ. (22mL)

    Clean001

  • INGREDIENTS AND APPEARANCE
    CLEAN AND CLEAR ADVANTAGE ACNE SPOT TREATMENT 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0126
    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)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    ALCOHOL (UNII: 3K9958V90M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    PPG-2 ISOCETETH-20 ACETATE (UNII: BI6C7YO419)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    LAURETH-7 (UNII: Z95S6G8201)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    AMMONIA (UNII: 5138Q19F1X)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    SARCOSINE (UNII: Z711V88R5F)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)  
    PURSLANE (UNII: M6S840WXG5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0126-11 in 1 CARTON10/01/2006
    122 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D10/01/2006
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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