Label: JASON DANDRUFF RELIEF TREATMENT 2 IN 1- zinc pyrithione shampoo
- NDC Code(s): 61995-0029-2
- Packager: The Hain Celestial Group, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2023
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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, Glycerin, Cetyl Alcohol, Cocamidopropyl Hydroxysultaine, Sodium Cocoyl Glutamate, Sodium Laurylglucosides Hydroxypropylsulfonate, Sodium Chloride, Glyceryl Stearate SE, Coco-Glucoside, Glyceryl Oleate, Butyrospermum Parkii (Shea) Butter Unsaponifiables, Cannabis Sativa Seed Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Citrus Nobilis (Mandarin Orange) Peel Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Juniperus Mexicana Oil, Myristica fragrans (Nutmeg) kernel oil, Olea Europaea (Olive) Fruit Oil (1), Pelargonium Graveolens Flower Oil, Pimpinella Anisum (Anise) Seed Oil, Pogostemon Cablin Oil, Simmondsia Chinensis (Jojoba) Seed Oil (1), Soybean Glycerides, Zingiber Officinale (Ginger) Root Oil, Aloe Barbadensis Leaf Juice (1), Cannabis Sativa Seed Extract, Chenopodium Quinoa Seed (1), Leuconostoc/Radish Root Ferment Filtrate, Ascorbyl Palmitate, Babassu Oil Polyglyceryl-4 Esters, Caprylic/Capric Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Cellulose Gum, Citric Acid, Diheptyl Succinate, Guar Hydroxypropyltrimonium Chloride, Sodium Hydroxide, Sodium PCA, Xanthan Gum, Zinc Carbonate, Alcohol (1), Ethylhexylglycerin, Phenoxyethanol, Potassium Sorbate, Benzyl Salicylate, Fragrance (Natural), Limonene, Linalool.
(1) Certified Organic Ingredients
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INGREDIENTS AND APPEARANCE
JASON DANDRUFF RELIEF TREATMENT 2 IN 1
zinc pyrithione shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-0029 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 WATER (UNII: 059QF0KO0R) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) GLYCERIN (UNII: PDC6A3C0OX) SODIUM COCO-SULFATE (UNII: 3599J29ANH) GLYCOL STEARATE (UNII: 0324G66D0E) CETYL ALCOHOL (UNII: 936JST6JCN) BABASSU OIL (UNII: 8QSB4M5477) OLIVE OIL (UNII: 6UYK2W1W1E) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) JOJOBA OIL (UNII: 724GKU717M) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) ZINC CARBONATE (UNII: EQR32Y7H0M) POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO) ALOE VERA LEAF (UNII: ZY81Z83H0X) NUTMEG OIL (UNII: Z1CLM48948) GINGER OIL (UNII: SAS9Z1SVUK) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) ANISE OIL (UNII: 6Y89129C8H) PEG-4 CAPRYLIC/CAPRIC GLYCERIDES (UNII: H45189YI2Q) XANTHAN GUM (UNII: TTV12P4NEE) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) CITRIC ACID ACETATE (UNII: DSO12WL7AU) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SODIUM CHLORIDE (UNII: 451W47IQ8X) SHEA BUTTER (UNII: K49155WL9Y) LEMON PEEL (UNII: 72O054U628) CLOVE LEAF OIL (UNII: VCA5491KVF) CANNABIS SATIVA SEED (UNII: QE567Z26NG) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LINALOOL, (+)- (UNII: F4VNO44C09) BENZYL SALICYLATE (UNII: WAO5MNK9TU) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) ALCOHOL 95% (UNII: 7528N5H79B) ASCORBYL PALMITATE (UNII: QN83US2B0N) ORANGE PEEL (UNII: TI9T76XD44) MANDARIN OIL (UNII: NJO720F72R) JUNIPERUS OXYCEDRUS LEAF OIL (UNII: YNW2QPG8YK) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) QUINOA OIL (UNII: M437LS0K52) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) LIMONENE, (+)- (UNII: GFD7C86Q1W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61995-0029-2 355 g in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 04/19/2012 Labeler - The Hain Celestial Group, Inc (117115556) Registrant - The Hain Celestial Group, Inc. (014334364) Establishment Name Address ID/FEI Business Operations The Hain Celestial Group, Inc 081512382 manufacture(61995-0029)
