Label: CLEAR COMPLETE SCALP CARE ANTIDANDRUFF CONDITIONER- pyrithione zinc suspension
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1435-1 - Packager: Conopco Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated September 22, 2015
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients
Water (Aqua), Cetearyl Alcohol, Cyclopentasiloxane, Stearamidopropyl Dimethylamine, Dimethiconol, Behentrimonium Chloride, Fragrance (Parfum), Dipropylene Glycol, Lactic Acid, DMDM Hydantoin, Zinc Sulfate, Sodium Chloride, TEA-Dodecylbenzenesulfonate, Elaeis Guineensis (Palm) Oil, Helianthus Annuus (Sunflower) Seed Oil, Aloe Barbadensis Leaf Juice, Glycerin, Butylene Glycol, Iodopropynyl Butylcarbamate, Glycine Soja (Soybean) Oil, Cucumis Sativus (Cucumber) Fruit Extract, Methylisothiazolinone, Ascorbic Acid, Panthenol, Tocopheryl Acetate, Mentha Piperita (Peppermint) Oil, Methylchloroisothiazolinone, Biotin, Niacinamide.
- QUESTIONS
- 12.7 fl oz PDP
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INGREDIENTS AND APPEARANCE
CLEAR COMPLETE SCALP CARE ANTIDANDRUFF CONDITIONER
pyrithione zinc suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1435 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Pyrithione Zinc (UNII: R953O2RHZ5) (Pyrithione Zinc - UNII:R953O2RHZ5) Pyrithione Zinc 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) DMDM HYDANTOIN (UNII: BYR0546TOW) TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN) DIPROPYLENE GLYCOL (UNII: E107L85C40) LACTIC ACID (UNII: 33X04XA5AT) ZINC SULFATE (UNII: 89DS0H96TB) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) PEPPERMINT OIL (UNII: AV092KU4JH) SUNFLOWER OIL (UNII: 3W1JG795YI) PALM OIL (UNII: 5QUO05548Z) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW) ASCORBIC ACID (UNII: PQ6CK8PD0R) PANTHENOL (UNII: WV9CM0O67Z) BIOTIN (UNII: 6SO6U10H04) NIACINAMIDE (UNII: 25X51I8RD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1435-1 375 mL in 1 CONTAINER; 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 12/15/2015 Labeler - Conopco Inc. d/b/a Unilever (001375088) Establishment Name Address ID/FEI Business Operations Unilever Supply Chain Co. d/b/a Unilever 043510056 manufacture(64942-1435)