Label: NEUTROGENA RAPID CLEAR 2 IN 1 FIGHT AND FADE TONER- salicylic acid solution

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

Drug Label Information

Updated November 11, 2024

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

  • 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 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

    • Cleanse 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., butylene glycol, PPG-5-ceteth-20, C12-15 alkyl lactate, sodium citrate, fragrance, cocamidopropyl PG-dimonium chloride phosphate, PEG/PPG-20/6 dimethicone, cetyl lactate, benzalkonium chloride, sodium benzotriazolyl butylphenol sulfonate, disodium EDTA, sodium hydroxide, glycolic acid, yellow 6, red 40

  • Questions?

    Call toll free 800-582-4048 or 215-273-8755 (collect) www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

    NEUTORGENA
    Rapid
    Clear ®
    2-in-1
    Fight & Fade Toner

    MICRO CLEAR®
    technology

    FIGHTS
    breakouts
    in under
    8 hours
    FADES
    the look of
    post-acne
    marks

    Neutrogena ®

    salicylic acid acne treatment
    8 FL. OZ. (236mL)

    PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA RAPID CLEAR 2 IN 1 FIGHT AND FADE TONER 
    salicylic acid solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0158
    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)  
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    PEG/PPG-20/6 DIMETHICONE (UNII: PWZ7N4UIKE)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0158-8236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00610/01/2009
    Labeler - Kenvue Brands LLC (118772437)