NEUTROGENA OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB- 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 pink grapefruit foaming scrub

Drug Facts

Active ingredients

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.

Other information

Store at Room Temperature

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Microcrystalline Cellulose, Sodium Chloride, Acrylates Copolymer, Cellulose, Polysorbate 20, Fragrance, C12-15 Alkyl Lactate, Sodium Hydroxide, Disodium EDTA, Benzalkonium Chloride, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Benzotriazolyl Butylphenol Sulfonate, Propylene Glycol, Citrus Grandis (Grapefruit) Fruit Extract, Carrageenan, Agar, Ascorbyl Palmitate, Mica, Titanium Dioxide, Red 30, Red 40, Violet 2

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 - 198 mL Tube Label

VALUE SIZE

Oil-Free

Acne Wash

pink grape fruit

foaming scrub

MICRO CLEAR ®

technology

clear breakouts

naturally derived grapefruit extract

Neutrogena ®

salicylic acid acne treatment

6.7 FL. OZ. (198 mL)

Ntg_001

NEUTROGENA OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0610
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PUMMELO (UNII: ET1TN5W71X)  
CARRAGEENAN (UNII: 5C69YCD2YJ)  
AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
MICA (UNII: V8A1AW0880)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
D&C RED NO. 30 (UNII: 2S42T2808B)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0610-7198 mL in 1 TUBE; Type 0: Not a Combination Product12/30/2019
2NDC:69968-0610-4124 mL in 1 TUBE; Type 0: Not a Combination Product12/30/2019
3NDC:69968-0610-259 mL in 1 TUBE; Type 0: Not a Combination Product12/09/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D12/09/2019
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 3/2023
Document Id: f640d50c-1aa6-96c1-e053-2995a90a543e
Set id: 6b2e27a6-961f-4f5c-a834-fcbd23460e68
Version: 8
Effective Time: 20230306
 
Johnson & Johnson Consumer Inc.