NEUTROGENA SCALP THERAPY ANTI-DANDRUFF DAILY CONTROL- salicylic acid shampoo

Neutrogena Scalp Therapy Anti-Dandruff Daily Control by

Drug Labeling and Warnings

Neutrogena Scalp Therapy Anti-Dandruff Daily Control 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 (1.8%)

Purposes

Anti-dandruff, Anti-seborrheic dermatitis, Anti-psoriasis

Use

Controls the symptoms of dandruff, seborrheic dermatitis and psoriasis.

Warnings

• For external use only.

• Ask a doctor before use if you have a condition that covers a large area of the body.

• When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

• Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.

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

Directions

• For best results, use at least twice a week or as directed by a doctor.
• Wet hair thoroughly.
• Massage shampoo into your scalp.
• Lather, leaving on your hair and scalp for a few minutes.
• Rinse and repeat.

Other information

Store at room temperature.

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, Polyquaternium-22, Sodium Citrate, Hexylene Glycol, Sodium Lauroyl Sarcosinate, Fragrance, Linoleamidopropyl PG-Dimonium Chloride Phosphate, Citric Acid, Sodium Hydroxide

Questions?

Call 800-256-4247 or 215-273-8755 (collec t) or visit www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 354 mL Bottle Carton

NEUTROGENA

Scalp Therapy TM

Anti-Dandruff

MEDICATED

DAILY CONTROL

1.8% SALICYLIC ACID

SHAMPOO

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

12 FL OZ (354 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA SCALP THERAPY ANTI-DANDRUFF DAILY CONTROL 
salicylic acid shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0722
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	18 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
LINOLEAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0722-1	354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	12/06/2021

Labeler - Johnson & Johnson Consumer Inc. (118772437)