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

  • NDC Code(s): 69968-0472-1
  • 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 6, 2023

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 occour if you use another tropical 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

    • cleanse the skin thoroughly before applying product.
    • cover the entire affected area with a thin layer 1-3 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 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 a 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, cyclopentasiloxane, C13-14 isoparaffin, C12-15 alkyl lactate, alcohol, phenoxyethanol, cetyl lactate, PPG-2 isoceteth-20 acetate, cocamidopropyl PG-dimonium chloride phosphate, laureth-7, polysorbate 20, phenethyl dimethicone, fragrance, dehydroxanthan gum, propylene glycol, benzalkonium chloride, ammonia, 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 US , 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

    NEW LOOK

    NEUTROGENA
    Rapid
    Clear®

    Acne
    Eliminating
    Spot Gel

    MICRO CLEAR®
    technology

    Neutrogena ®

    salicylic acid acne treatment

    0.5 FL OZ (15mL)

    PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0472
    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)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    ALCOHOL (UNII: 3K9958V90M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    PPG-2 ISOCETETH-20 ACETATE (UNII: BI6C7YO419)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    LAURETH-7 (UNII: Z95S6G8201)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    AMMONIA (UNII: 5138Q19F1X)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0472-11 in 1 CARTON10/30/2019
    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 finalpart333D10/30/2019
    Labeler - Johnson & Johnson Consumer Inc. (118772437)