Label: BREAKOUT CLEARING BOOSTER- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2025

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Salicylic Acid (2.0%)

  • Purpose

    Acne Treatment

  • Use

    • For the treatment of acne
  • Warnings

    For external use only

    Do not use

    • In or near eyes. If contact occurs, flush thoroughly with water.
    • If irritation or redness develops, discontinue use.

    When using this product

    • apply to affected areas only.
    • skin irritation and dryness are 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

    • 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.
  • Inactive Ingredients

    Water/Aqua/Eau, PPG-15 Stearyl Ether, Butylene Glycol, Glycerin, Isopropyl Lauroyl Sarcosinate, Niacinamide, Cetearyl Glucoside, Polysorbate 20, 1,2-Hexanediol, Hydroxyacetophenone, Lactic Acid, Sodium Hyaluronate, Citrus Aurantium Dulcis (Orange) Peel Oil, Chlorella Vulgaris Extract, Chondrus Crispus Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Coconut Alkanes, Sclerotium Gum, Coco-Caprylate/Caprate, Xanthan Gum, Glyceryl Stearate, PEG-100 Stearate, Tetrasodium Glutamate Diacetate, Sodium Hydroxide, Propanediol, Sodium Citrate, Terpineol, Thymol, Limonene.

  • Questions or comments

    Call toll free 1-800-831-5150 in the US

  • PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton

    clears breakout
    causing bacteria in
    15 minutes

    breakout clearing
    booster

    dermatologica
    clear start

    targeted spot treatment

    1.0 US FL OZ / 30 mL ℮

    PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    BREAKOUT CLEARING BOOSTER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-773
    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)  
    Polypropylene Glycol 15 Stearyl Ether (UNII: 1II18XLS1L)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Glycerin (UNII: PDC6A3C0OX)  
    Isopropyl Lauroyl Sarcosinate (UNII: LYR06W430J)  
    Niacinamide (UNII: 25X51I8RD4)  
    Cetearyl Glucoside (UNII: 09FUA47KNA)  
    Polysorbate 20 (UNII: 7T1F30V5YH)  
    1,2-Hexanediol (UNII: TR046Y3K1G)  
    Hydroxyacetophenone (UNII: G1L3HT4CMH)  
    Coconut Alkanes (UNII: 1E5KJY107T)  
    Betasizofiran (UNII: 2X51AD1X3T)  
    Glyceryl Monostearate (UNII: 230OU9XXE4)  
    PEG-100 MONOSTEARATE (UNII: YD01N1999R)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    Propanediol (UNII: 5965N8W85T)  
    Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
    CHONDRUS CRISPUS (UNII: OQS23HUA1X)  
    Orange Oil, Cold Pressed (UNII: AKN3KSD11B)  
    Terpineol (UNII: R53Q4ZWC99)  
    Thymol (UNII: 3J50XA376E)  
    Tetrasodium Glutamate Diacetate (UNII: 5EHL50I4MY)  
    Cocoyl Caprylocaprate (UNII: 8D9H4QU99H)  
    Chlorella Vulgaris (UNII: RYQ4R60M02)  
    LACTIC ACID, DL- (UNII: 3B8D35Y7S4)  
    Hyaluronate Sodium (UNII: YSE9PPT4TH)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Limonene, (+)- (UNII: GFD7C86Q1W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68479-773-021 in 1 CARTON11/12/2025
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00611/12/2025
    Labeler - Dermalogica, LLC. (177698560)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosway052400223MANUFACTURE(68479-773)
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