Label: J1003005 JASON DANDRUFF RELIEF- sulfur, salicylic acid shampoo
- NDC Code(s): 61995-0030-8
- Packager: The Hain Celestial Group, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 31, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Water (Aqua), Potassium Cocoyl Glutamate, Sodium Cocoyl Isethionate, Cetyl Alcohol, Disodium Cocoamphodiacetate, Cocamidopropyl Betaine, Stearic Acid, Glycerin, Glyceryl Stearate SE, Sodium Laurylglucosides Hydroxypropylsulfonate, Olea Europaea (Olive) Fruit Oil (1), Rosmarinus Officinalis (Rosemary) Leaf Oil, Simmondsia Chinensis (Jojoba) Seed Oil (1), Chenopodium Quinoa Seed (1), Camphor, Capryloyl Glycine, Disodium Cocoyl Glutamate, Maltodextrin, Menthol, Methyl Salicylate, Potassium Hydroxide, Sodium Chloride, Sodium PCA, Triethyl Citrate, Undecylenoyl Glycine, Xanthan Gum, Alcohol (1), Benzyl Alcohol, Linalool
(1) Certified Organic Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
J1003005 JASON DANDRUFF RELIEF
sulfur, salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-0030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 2.4 g in 100 g SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2.2 g in 100 g Inactive Ingredients Ingredient Name Strength SODIUM LAURYLGLUCOSIDES HYDROXYPROPYLSULFONATE (UNII: Z6GFR7R72Y) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X) WATER (UNII: 059QF0KO0R) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) MALTODEXTRIN (UNII: 7CVR7L4A2D) OLIVE OIL (UNII: 6UYK2W1W1E) ROSEMARY OIL (UNII: 8LGU7VM393) JOJOBA OIL (UNII: 724GKU717M) CAMPHOR (NATURAL) (UNII: N20HL7Q941) MENTHOL (UNII: L7T10EIP3A) METHYL SALICYLATE (UNII: LAV5U5022Y) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) XANTHAN GUM (UNII: TTV12P4NEE) BENZYL ALCOHOL (UNII: LKG8494WBH) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) UNDECYLENOYL GLYCINE (UNII: 4D20464K2J) LINALOOL, (+/-)- (UNII: D81QY6I88E) ALCOHOL (UNII: 3K9958V90M) POTASSIUM COCOYL GLUTAMATE (UNII: IR5T90R7LZ) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) SODIUM CHLORIDE (UNII: 451W47IQ8X) DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61995-0030-8 355 g in 1 BOTTLE; Type 0: Not a Combination Product 11/27/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/27/2017 Labeler - The Hain Celestial Group, Inc. (117115556) Registrant - The Hain Celestial Group, Inc. (081512382)
