NEUTROGENA T/SAL THERAPEUTIC- salicylic acid shampoo

Neutrogena T/Sal by

Drug Labeling and Warnings

Neutrogena T/Sal 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 3.0%

Purpose

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 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 physician
• Wet hair thoroughly
• Massage liberal amount of shampoo into the scalp
• Leave lather on scalp for several minutes
• Rinse and repeat

Inactive ingredients

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

Questions or comments?

Call 1-877-256-4247 (USA only). For more information go to: www.tgel.com

SPL UNCLASSIFIED SECTION

© Dist. by Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 133 mL Carton

Neutrogena®
T/SAL®
therapeutic
shampoo

Scalp Build-Up
Control

clears and helps
prevent flakes and
scalp build-up

• starts working after
  just one use
• dandruff, psoriasis,
  seborrheic dermatitis

#1 DERMATOLOGIST
RECOMMENDED BRAND

NEUTROGENA®

3% SALICYLIC ACID
4.5 FL OZ (133mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA T/SAL   THERAPEUTIC
salicylic acid shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-916
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Linoleamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: 5Q87K461JO)
Sodium Lauroyl Sarcosinate (UNII: 632GS99618)
Hexylene Glycol (UNII: KEH0A3F75J)
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-916-02	1 in 1 CARTON	10/12/2011
1		133 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 10812-916-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/12/2011
3	NDC: 10812-916-67	12 in 1 CARTON	10/12/2011
3		29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part358H	10/12/2011

Labeler - Johnson & Johnson Consumer Inc. (002347102)