Neutrogena Oil-Free Acne Stress Control Power-Cream Wash

Neutrogena Oil Free Acne Stress Control by

Drug Labeling and Warnings

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

Drug Details [pdf]

NEUTROGENA OIL FREE ACNE STRESS CONTROL- salicylic acid cream 
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 Power-Cream Wash

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 face twice a day.
• Wet face and squeeze cleanser into hands.
• Apply to face and massage gently, avoiding contact with delicate eye area.
• Rinse thoroughly.

Other information

Store at Room Temperature.

Inactive ingredients

Water, Cetyl Alcohol, PPG-15 Stearyl Ether, Glycolic Acid, Glycerin, Polysorbate 60, C12-15 Alkyl Lactate, Cetyl Lactate, Potassium Cetyl Phosphate, Sodium Hydroxide, Fragrance, Cocamidopropyl PG-Dimonium Chloride Phosphate, Xanthan Gum, Disodium EDTA, Menthol, Benzalkonium Chloride, Panthenol, Butylene Glycol, Camellia Oleifera Leaf Extract, Cucumus Sativus (Cucumber) Fruit Extract, Green 5, Yellow 5, Blue 1

Questions?

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

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.

Dist. by Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 177 mL Tube Label

NEW INFO

Oil-Free
Acne Stress
Control®

Power-Cream Wash

MICROCLEAR®

technology

Treats acne even
before it emerges

Neutrogena®
salicylic acid acne treatment

6 FL. OZ. (177 mL)

NEUTROGENA OIL FREE ACNE STRESS CONTROL 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-268
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)
Cetyl Alcohol (UNII: 936JST6JCN)
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
GLYCOLIC ACID (UNII: 0WT12SX38S)
Glycerin (UNII: PDC6A3C0OX)
Polysorbate 60 (UNII: CAL22UVI4M)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
CETYL LACTATE (UNII: A7EVH2RK4O)
Steareth-21 (UNII: 53J3F32P58)
cocamidopropyl propylene glycol-dimonium chloride phosphate (UNII: H2KVQ74JM4)
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)
Edetate Disodium (UNII: 7FLD91C86K)
Xanthan Gum (UNII: TTV12P4NEE)
sodium Hydroxide (UNII: 55X04QC32I)
Panthenol (UNII: WV9CM0O67Z)
Camellia Oleifera Leaf (UNII: 5077EL0C60)
CUCUMBER (UNII: YY7C30VXJT)
Butylene Glycol (UNII: 3XUS85K0RA)
Menthol, unspecified form (UNII: L7T10EIP3A)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Fd&C Yellow No. 5 (UNII: I753WB2F1M)
D&C Green No. 5 (UNII: 8J6RDU8L9X)
Fd&C Blue No. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-268-01	177 mL in 1 TUBE; Type 0: Not a Combination Product	05/01/2011	09/29/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	05/01/2011	09/29/2011

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 3/2020

Document Id: 6882131b-578c-4285-8f39-11c681e98b67

34390-5

Set id: 5deffb03-07d9-458f-b66d-7d0d4ba050af

Version: 5

Effective Time: 20200323

 

Johnson & Johnson Consumer Inc.