Label: NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT- salicylic acid gel

  • NDC Code(s): 69968-0825-1
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 29, 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 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 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

    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.

    Store at Room Temperature.

  • Inactive ingredients

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

  • Questions?

    800-299-4786; Outside US, dial collect 215-273-8755 or www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

    Distributed by:

    JOHNSON & JOHNSON

    CONSUMER INC.

    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton

    NEUTROGENA

    Rapid

    Clear ®

    Acne

    Eliminating

    Spot Gel

    MICROCLEAR®

    technology

    Neutrogena®

    salicylic acid acne treatment

    0.5 FL OZ (15mL)

    Neutrogena_01

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0825
    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
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    SARCOSINE (UNII: Z711V88R5F)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)  
    PURSLANE (UNII: M6S840WXG5)  
    WATER (UNII: 059QF0KO0R)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    ALCOHOL (UNII: 3K9958V90M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    LAURETH-7 (UNII: Z95S6G8201)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0825-11 in 1 CARTON08/30/2023
    115 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/30/2023
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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