NEUTROGENA OIL FREE ACNE WASH- salicylic acid liquid 
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

Other information

Store at Room Temperature.

Inactive ingredients

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

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 269 mL Bottle Label

Oil-Free
Acne Wash
MICRO CLEAR ®
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 liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0675
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)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CHAMOMILE (UNII: FGL3685T2X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0675-112 in 1 TRAY07/13/2020
114 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:69968-0675-6177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/13/2020
3NDC:69968-0675-9269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D07/13/2020
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ef17cfe5-8b52-8530-e053-2995a90a4571
Set id: c4775032-9723-4208-8a42-145f2b4da1c8
Version: 4
Effective Time: 20230112
 
Johnson & Johnson Consumer Inc.