NEUTROGENA CLEAR PORE OIL-ELIMINATING ASTRINGENT- 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 ® Clear Pore Oil-Eliminating Astringent

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Use

For the treatment of acne.

Warnings

For external use only.

Flammable: Keep away from fire or flame.

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.
  • if eye 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

Alcohol Denat., Water, Hamamelis Virginiana (Witch Hazel) Water, Butylene Glycol, Glycereth-7, Methyl Gluceth-20, Alcohol, Fragrance, Propylene Glycol, Benzophenone-4, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Blue 1

Questions?

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

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

Clear
Pore

Oil-Eliminating
Astringent

effectively treats
and helps prevent
breakouts without
overdrying

salicylic acid
acne medication

Neutrogena ®

DERMATOLOGIST RECOMMENDED

8 FL. OZ. (236 mL)

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label
NEUTROGENA CLEAR PORE OIL-ELIMINATING ASTRINGENT 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0028
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
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCERETH-7 (UNII: 3D2Y91QZ2H)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SULISOBENZONE (UNII: 1W6L629B4K)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CHAMOMILE (UNII: FGL3685T2X)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0028-8236 mL in 1 BOTTLE; Type 0: Not a Combination Product01/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/31/2020
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ee331a9e-ed16-24ad-e053-2a95a90a5b3b
Set id: 107ad1a9-0da7-4002-a40d-cee3764c6f6b
Version: 3
Effective Time: 20230105
 
Johnson & Johnson Consumer Inc.