NEUTROGENA ACNE PROOFING DAILY 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 Acne Proofing daily scrub

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 Rome Temperature

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Acrylates Crosspolymer-4, Panthenol, Sodium Hydroxide, Fragrance, Microcrystalline Wax, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Cocamidopropyl PG-Dimonium Chloride Phosphate, Talc, Yellow 5 Lake, Red 30

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 - 119 g Tube Label

NEW

Acne
Proofing™
daily scrub
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 . 4.2 OZ. (119 g)

PRINCIPAL DISPLAY PANEL - 119 g Tube Label
NEUTROGENA ACNE PROOFING DAILY SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0112
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)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
SORBITOL (UNII: 506T60A25R)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
PANTHENOL (UNII: WV9CM0O67Z)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
D&C RED NO. 30 (UNII: 2S42T2808B)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
TALC (UNII: 7SEV7J4R1U)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0112-4119 g in 1 TUBE; Type 0: Not a Combination Product10/01/201705/22/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D10/01/201705/22/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 6/2023
Document Id: fd81dd4b-9616-f4c1-e053-6394a90a5e72
Set id: d9cc3a57-4da5-4d94-a445-a38f88692c84
Version: 5
Effective Time: 20230606
 
Johnson & Johnson Consumer Inc.