NEUTROGENA STUBBORN BODY ACNE CLEANSER AND EXFOLIATOR- salicylic acid liquid

Neutrogena Stubborn Body Acne Cleanser and Exfoliator by

Drug Labeling and Warnings

Neutrogena Stubborn Body Acne Cleanser and Exfoliator by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Salicylic Acid (1%)

Purpose

Acne treatment

Use

For the treatment of acne.

Warnings

For external use only.

When using this product

• ▪ Avoid contact with eyes. If contact occurs, immediately flush with water.

  ▪ 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.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

▪ Wet body ▪ Gently massage over body for 20-30 seconds

▪ Rinse thoroughly ant pat dry

▪ Recommended for daily use

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Other Information

• Store at room temperature

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol, Gluconolactone, Sodium Hydroxide, Potassium Acrylates Copolymer, Disodium EDTA

Questions?

800-582-4048; Outside US, dial collect 215-273-8755 or visit www.neutrogena.com

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Distributed by:

JOHNSON & JOHNSON

CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 250mL Bottle

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

NEW

STUBBORN

BODY ACNE

CLEANSER & EXFOLIATOR

Salicylic Acid Acne Treatment

Salicylic Acid + PHA

Fragrance Free

gently exfoliates, clears & helps

prevent breakouts

8.5 FL OZ (250mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA STUBBORN BODY ACNE CLEANSER AND EXFOLIATOR 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0759
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLUCONOLACTONE (UNII: WQ29KQ9POT)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0759-8	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	08/01/2022

Labeler - Kenvue Brands LLC (118772437)