NEUTROGENA OIL FREE ACNE STRESS CONTROL TRIPLE ACTION TONER- salicylic acid liquid

Neutrogena Oil Free Acne Stress Control Triple Action Toner by

Drug Labeling and Warnings

Neutrogena Oil Free Acne Stress Control Triple Action Toner by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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 hydroxy 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, Camellia Sinensis Leaf Extract, Glycerin, Cucumis Sativus (Cucumber) Fruit Extract, Yellow 5, Blue 1, Green 5

Questions?

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label

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)

INGREDIENTS AND APPEARANCE

NEUTROGENA OIL FREE ACNE STRESS CONTROL TRIPLE ACTION TONER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0521
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Anhydrous (UNII: 8NLQ36F6MM)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Glycerin (UNII: PDC6A3C0OX)
Cucumber (UNII: YY7C30VXJT)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0521-8	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	03/01/2019

Labeler - Johnson & Johnson Consumer Inc. (002347102)