NEUTROGENA ACNE PROOFING CLEANSER- 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 Acne Proofing™ gel cleanser

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 lather. Massage face gently. Rinse thoroughly.

Inactive ingredients

Water, Cocamidopropyl Hydroxysultaine, Sodium Methyl Cocoyl Taurate, Sodium Chloride, Glycerin, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Fragrance, Sodium Hydroxide, PEG-120 Methyl Glucose Dioleate, Panthenol, C12-15 Alkyl Lactate, Disodium EDTA, Cocamidopropyl PG-Dimonium Chloride Phosphate, Benzalkonium Chloride

Other information

Store at room temperature.

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 170 g Bottle Label

NEW

Acne
Proofing™
gel cleanser

clears breakouts and helps
defend against new ones to make
skin more acne resistant

CLEARDEFEND
TECHNOLOGY™

maximum strength
salicylic acid acne treatment

Neutrogena ®

DERMATOLOGIST RECOMMENDED

NET WT. 6 OZ.
(170 g)

30034355

PRINCIPAL DISPLAY PANEL - 170 g Bottle Label
NEUTROGENA ACNE PROOFING CLEANSER 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
PANTHENOL (UNII: WV9CM0O67Z)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0110-114 g in 1 TUBE; Type 0: Not a Combination Product10/01/201712/28/2020
2NDC:69968-0110-6170 g in 1 BOTTLE; Type 0: Not a Combination Product10/01/201703/12/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D10/01/201703/12/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 3/2023
Document Id: f7897499-42b3-06c3-e053-6294a90af294
Set id: 6f8d1991-1f3b-4136-9525-4e4843afc62c
Version: 7
Effective Time: 20230322
 
Johnson & Johnson Consumer Inc.