NEUTROGENA OIL FREE ACNE WASH- salicylic acid gel 
Johnson & Johnson Consumer Inc.

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.

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Neutrogena® Oil-Free Acne Wash

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, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, PEG-80 Sorbitan Laurate, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Fragrance, Cocamidopropyl PG-Dimonium Chloride Phosphate, Propylene Glycol, Aloe Barbadensis Leaf Extract, Anthemis Nobilis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Sodium Hydroxide, Citric Acid, Yellow 5, Red 40

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 269 mL Bottle Label

Oil-Free
Acne Wash

MICROCLEAR®
technology

# 1 DERMATOLOGIST RECOMMENDED

Neutrogena®

salicylic acid acne treatment

9.1 FL. OZ. (269 mL)

Principal Display Panel - 269 mL Bottle Label
NEUTROGENA OIL FREE ACNE WASH 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0167
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)  
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
Sodium Chloride (UNII: 451W47IQ8X)  
PEG-80 Sorbitan Laurate (UNII: 239B50Y732)  
C12-15 Alkyl Lactate (UNII: GC844VRD7E)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)  
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Aloe Vera Leaf (UNII: ZY81Z83H0X)  
Chamaemelum Nobile Flower (UNII: O2T154T6OG)  
Chamomile (UNII: FGL3685T2X)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Fd&C Yellow No. 5 (UNII: I753WB2F1M)  
Fd&C Red No. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0167-9269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/01/200908/18/2019
2NDC:69968-0167-6177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/01/200908/21/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D02/01/200908/21/2019
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 8/2020
Document Id: 4b4285a3-a163-4324-9d7f-ab476dc9c6ef
Set id: eb80b0db-4a06-450e-b3a1-a16c71b1c41f
Version: 4
Effective Time: 20200814
 
Johnson & Johnson Consumer Inc.