Label: ACNE SOLUTIONS CLARIFYING- salicylic acid liquid

  • NDC Code(s): 49527-723-01, 49527-723-02, 49527-723-03
  • Packager: CLINIQUE LABORATORIES LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active ingredient

    Salicylic acid 1.5%

  • Purpose

    Acne treatment

  • Uses

    • treats acne
    • clears acne blemishes
    • helps prevent development of new acne blemishes
    • for the management 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 this 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

    • shake vigorously
    • using a cotton ball, sweep over face and throat, avoiding eye area
    • use AM and PM after Acne Solutions Cleansing Foam
    • if bothersome drying or peeling occurs, reduce usage to every other day
    • after acne clears, continue using for preventative care
    • follow with Acne Solutions All-Over Clearing Treatment
    • because excessive drying of the skin may occur, start with one use daily, then gradually increase to twice a day if needed or as directed by a doctor
  • Inactive ingredients

    water\aqua\eau,alcohol denat.,hamamelis virginiana (witch hazel) water,alcohol,nylon-12,butylene glycol,acetyl glucosamine,glycerin,laminaria saccharina extract,caffeine,sorbitol,10-hydroxydecanoic acid,silica,barium sulfate,sucrose,disodium edta,benzalkonium chloride <iln52764>

  • PRINCIPAL DISPLAY PANEL - 200 ml Bottle

    CLINIQUE

    acne solutions

    clarifying lotion

    STEP 2

    SALICYLIC ACID ACNE MEDICATION

    6.7 FL.OZ./200 ml e

    PDP

  • INGREDIENTS AND APPEARANCE
    ACNE SOLUTIONS CLARIFYING 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-723
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID15 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    NYLON-12 (UNII: 446U8J075B)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)  
    SACCHARINA LATISSIMA (UNII: 68CMP2MB55)  
    CAFFEINE (UNII: 3G6A5W338E)  
    SUCROSE (UNII: C151H8M554)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    N-ACETYLGLUCOSAMINE (UNII: V956696549)  
    SORBITOL (UNII: 506T60A25R)  
    PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)  
    BARIUM SULFATE (UNII: 25BB7EKE2E)  
    10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49527-723-021 in 1 CARTON03/02/2022
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49527-723-03100 mL in 1 BOTTLE; Type 0: Not a Combination Product10/20/2023
    3NDC:49527-723-01200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2006
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/01/2006
    Labeler - CLINIQUE LABORATORIES LLC (044475127)
    Registrant - Estee Lauder Companies Inc. (790802086)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Estee Lauder Inc802599436manufacture(49527-723) , pack(49527-723) , label(49527-723)
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