NEUTROGENA STUBBORN TEXTURE DAILY CLEANSER- salicylic acid gel 
Johnson & Johnson Consumer Inc.

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Neutrogena ® STUBBORN TEXTURE DAILY CLEANSER

Drug Facts

Active ingredient

Salicylic Acid 1%

Purpose

Acne treatment

Use

Warnings

For external use only.

When using this product

  • Avoid contact with eyes. If contact occurs, flush thoroughly with water.
  • 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.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol, Glycolic Acid, Gluconolactone, Sodium Hydroxide, Potassium Acrylates Copolymer, Disodium EDTA

Other information

Questions?

800-582-4048; Outside US, dial collect 215-273-8755 or visit www.neutrogena.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 186 mL Bottle Label

New
Neutrogena ®
DERMATOLOGIST RECOMMENDED BRAND

STUBBORN
TEXTURE
DAILY CLEANSER

Salicylic Acid Acne Treatment

clears acne & visibly
smooths uneven texture

4% Glycolic + Polyhydroxy Acids
Fragrance-Free

6.3 FL OZ (186mL)

PRINCIPAL DISPLAY PANEL - 186 mL Bottle Label
NEUTROGENA STUBBORN TEXTURE DAILY CLEANSER 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0704
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
SORBITOL (UNII: 506T60A25R)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0704-6186 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/02/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/02/2021
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 12/2023
Document Id: 0d1bc7a7-b2ab-5368-e063-6294a90ad3d9
Set id: ef2d9cd5-5c6c-4839-af5d-6bc21187b132
Version: 3
Effective Time: 20231222
 
Johnson & Johnson Consumer Inc.