Label: J1002901JASON DANDRUFF RELIEF 2IN1TREATMENT- zinc pyrithione shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 61995-0129-8 - Packager: The Hain Celestial Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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Drug Label Information
Updated April 12, 2021
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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), Sodium Cocoyl Isethionate, Cetyl Alcohol, Glycerin, Cocamidopropyl Hydroxysultaine, Sodium Laurylglucosides Hydroxypropylsulfonate, Sodium Cocoyl Glutamate, Sodium Chloride, Glyceryl Stearate SE, Coco-Glucoside, Glyceryl Oleate, Butyrospermum Parkii (Shea) Butter Unsaponifiables, Citrus Aurantium Dulcis (Orange) Peel Oil, Olea Europaea (Olive) Fruit Oil (1), Simmondsia Chinensis (Jojoba) Seed Oil (1), Soybean Glycerides, Chenopodium Quinoa Seed (1), Ascorbyl Palmitate, Babassu Oil Polyglyceryl-4 Esters, Benzyl Acetate, Caprylic/Capric Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Cellulose Gum, Citric Acid, Diheptyl Succinate, Guar Hydroxypropyltrimonium Chloride, Phenethyl Alcohol, Sodium Hydroxide, Sodium PCA, Terpineol, Triethyl Citrate, Xanthan Gum, Zinc Carbonate, Alcohol (1), Ethylhexylglycerin, Phenoxyethanol, Potassium Sorbate, Limonene, Linalool.
(1) Certified Organic Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
J1002901JASON DANDRUFF RELIEF 2IN1TREATMENT
zinc pyrithione shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-0129 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERYL OLEATE (UNII: 4PC054V79P) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) SODIUM DECYLGLUCOSIDES HYDROXYPROPYLSULFONATE (UNII: 55P9UXJ9C3) SODIUM HYDROXIDE (UNII: 55X04QC32I) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CAPRYLIC/CAPRIC ACID (UNII: DI775RT244) OLIVE OIL (UNII: 6UYK2W1W1E) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) TERPINEOL (UNII: R53Q4ZWC99) XANTHAN GUM (UNII: TTV12P4NEE) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) WATER (UNII: 059QF0KO0R) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) BABASSU OIL (UNII: 8QSB4M5477) JOJOBA OIL (UNII: 724GKU717M) ZINC CARBONATE (UNII: EQR32Y7H0M) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) ASCORBYL PALMITATE (UNII: QN83US2B0N) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SODIUM CHLORIDE (UNII: 451W47IQ8X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ORANGE OIL (UNII: AKN3KSD11B) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X) ALCOHOL (UNII: 3K9958V90M) BENZYL ACETATE (UNII: 0ECG3V79ZJ) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) ORANGE PEEL (UNII: TI9T76XD44) COCO GLUCOSIDE (UNII: ICS790225B) SHEA BUTTER (UNII: K49155WL9Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61995-0129-8 355 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 final part358H 11/27/2017 Labeler - The Hain Celestial Group, Inc. (117115556) Registrant - The Hain Celestial Group, Inc. (081512382) Establishment Name Address ID/FEI Business Operations The Hain Celestial Group, Inc 081512382 manufacture(61995-0129)