Label: NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - DEEP 20- salicylic acid liquid

  • NDC Code(s): 69968-0338-1
  • 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 16, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic Acid 0.5%

  • Purpose

    Acne medication

  • Use

    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.

    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

  • Inactive ingredients

    Water, cyclopentasiloxane, dimethicone, kaolin, VP/hexadecene copolymer, synthetic wax, cetyl PEG/PPG-10/1 dimethicone, trisiloxane, BIS-PEG/PPG-14/14 dimethicone, cyclohexasiloxane, butylene glycol, silica, phenoxyethanol, boron nitride, polysilicone-11, quaternium-90 bentonite, sodium chloride, magnesium sulfate, methylparaben, farnesol, chamomilla recutita (matricaria) flower extract, propylene carbonate, triethoxycaprylylsilane, propylparaben, aloe barbadensis leaf juice, polymethyl methacrylate, tocopheryl acetate, cocamidopropyl PG-dimonium chloride phosphate, cetyl lactate, C12-15 alkyl lactate, benzalkonium chloride, retinyl palmitate, pantothenic acid, ascorbic acid,titanium dioxide, iron oxides

  • Questions?

    Call toll-free 800-480-4812 or 215-273-8755 (collect) or visit www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 1.4 g Vial Blister Pack

    NEW
    DEEP
    20

    SkinClearing
    blemish concealer

    Don't just
    cover up.
    Clear up!
    with
    MICRO CLEAR®
    ------technology---------
    Blemish
    treatment
    with
    Salicylic
    Acid

    Conceals
    and treats
    blemishes

    Natural-
    looking
    coverage
    Neutrogena®
    NET WT
    0.05 OZ.
    (1.4g)

    PRINCIPAL DISPLAY PANEL - 1.4 g Vial Blister Pack
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA  SKIN CLEARING BLEMISH CONCEALER - DEEP 20
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0338
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    KAOLIN (UNII: 24H4NWX5CO)  
    VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BORON NITRIDE (UNII: 2U4T60A6YD)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    FARNESOL (UNII: EB41QIU6JL)  
    CHAMOMILE (UNII: FGL3685T2X)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    PANTOTHENIC ACID (UNII: 19F5HK2737)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    QUATERNIUM-90 BENTONITE (UNII: 97K5YEF88C)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0338-11.4 in 1 BLISTER PACK10/02/2017
    11.4 g in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D10/02/2017
    Labeler - Johnson & Johnson Consumer Inc. (118772437)