NEUTROGENA T/Sal therapeutic shampoo Drug Facts Active ingredient Salicylic Acid (3%) 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 physician . Wet hair thoroughly. Massage liberal amount into the scalp. Leave lather on scalp for several 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, , Linoleamidopropyl PG-Dimonium Chloride Phosphate, Sodium Hydroxide, Citric Acid Questions? 877-256-4247 ; Outside US, dial collect 215-273-8755 www.neutrogena.com Distributed by: JOHNSON & JOHNSON CONSUMER INC. Skillman, NJ 08558 PRINCIPAL DISPLAY PANEL - 133 mL Bottle 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 DERMATOLOGIST RECOMMENDED BRAND Neutrogena 3% SALICYLIC ACID 4.5 FL. OZ. (133 mL) ® Johnson & Johnson Consumer Inc. NEUTROGENA T/SAL THERAPEUTIC salicylic acid shampoo Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0434 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) 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:69968-0434-4 1 in 1 CARTON 02/06/2020 1 133 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69968-0434-1 12 in 1 TRAY 09/01/2020 2 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 02/06/2020 Labeler - Johnson & Johnson Consumer Inc. (118772437) Revised: 1/2023