Label: NEUTROGENA ALL IN 1 ACNE CONTROL DAILY SCRUB- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 11, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic Acid 2%

  • Purpose

    Acne treatment

  • 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.
    • avoid contact with eyes. If 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 twice a day. Wet face. Apply to hands, add water and work into a lather. Massage face gently. Rinse thoroughly.

  • Other Information

    Store at Room Temperature.

  • Inactive ingredients

    water, cetyl alcohol, PPG-15 stearyl ether, cellulose, glycerin, Polysorbate 60, steareth-21, potassium cetyl phosphate, xanthan gum, fragrance, disodium EDTA, menthyl lactate, sodium hydroxide

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

    NEW &
    IMPROVED

    All-in-1
    Acne
    Control
    daily scrub

    works on acne's
    past, present & future

    • exfoliates past acne marks
    • clears present breakouts
    • helps prevent future breakouts

    Neutrogena ®

    salicylic acid acne treatment

    4.2 FL. OZ. (124mL)

    PRINCIPAL DISPLAY PANEL - 124 mL Tube Label
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA ALL IN 1 ACNE CONTROL DAILY SCRUB 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0092
    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)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    STEARETH-21 (UNII: 53J3F32P58)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0092-4124 mL in 1 TUBE; Type 0: Not a Combination Product06/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/01/2016
    Labeler - Kenvue Brands LLC (118772437)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!