NEUTROGENA OIL FREE ACNE STRESS CONTROL TRIPLE ACTION TONER- 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® Oil - Free Acne Stress Control® Triple - Action Toner

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne medication

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

  • cleanse skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

Store at Room Temperature.

Sunburn Alert

This product contains an alpha hydroxyl acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards.

Inactive ingredients

Water, Alcohol Denat., Butylene Glycol, PPG-5-Ceteth-20, C12-15 Alkyl Lactate, Fragrance, Sodium Citrate, Cocamidopropyl PG-Dimonium Chloride Phosphate, PEG/PPG-20/6 Dimethicone, Sodium Hydroxide, Benzalkonium Chloride, Cetyl Lactate, Sodium Benzotriazolyl Butylphenol Sulfonate, Disodium EDTA, Propylene Glycol, Cucumis Sativus (Cucumber) Fruit Extract, Camellia Oleifera Leaf Extract, Blue 1, Green 5, Yellow 5

Questions?

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

Dist. by Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label

NEW INFO
Oil-Free
Acne Stress
Control®

Triple-Action Toner

MICROCLEAR®
technology

1
Treats acne even
before
it emerges
2
Eliminates oil & shine
3
Refreshes & soothes

Neutrogena®

salicylic acid acne treatment

8 FL. OZ. (237mL)

Principal Display Panel - 237 mL Bottle Label
NEUTROGENA OIL FREE ACNE STRESS CONTROL TRIPLE ACTION TONER 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-285
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)  
Alcohol (UNII: 3K9958V90M)  
Butylene Glycol (UNII: 3XUS85K0RA)  
PPG-5-Ceteth-20 (UNII: 4AAN25P8P4)  
C12-15 Alkyl Lactate (UNII: GC844VRD7E)  
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
PEG/PPG-20/6 Dimethicone (UNII: PWZ7N4UIKE)  
SOdium Hydroxide (UNII: 55X04QC32I)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Cetyl Lactate (UNII: A7EVH2RK4O)  
Sodium Benzotriazolyl Butylphenol Sulfonate (UNII: 0LA2QC9O3Z)  
Edetate Disodium (UNII: 7FLD91C86K)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Cucumber (UNII: YY7C30VXJT)  
Camellia Oleifera Leaf (UNII: 5077EL0C60)  
Fd&C Blue No. 1 (UNII: H3R47K3TBD)  
D&C Green No. 5 (UNII: 8J6RDU8L9X)  
Fd&C Yellow No. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-285-02237 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/200806/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D05/01/200806/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 6/2016
 
Johnson & Johnson Consumer Inc.