Label: NIOXIN SCALP RECOVERY MEDICATING CLEANSER- pyrithione zinc lotion
- NDC Code(s): 69282-007-10, 69282-007-20, 69282-007-50
- Packager: The Wella Corporation
- 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 December 21, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive ingredients
WATER, STEARYL ALCOHOL, CETYL ALCOHOL, STEARAMIDOPROPYL DIMETHYLAMINE, DIMETHICONE, GLUTAMIC ACID, BENZYL ALCOHOL, PHENOXYETHANOL, FRAGRANCE, PROPYLPARABEN, METHYLPARABEN, CITRIC ACID, MENTHA PIPERITA (PEPPERMINT) OIL, MENTHA ARVENSIS LEAF OIL, MENTHOL, YEAST EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, LECITHIN, PPG-26-BUTETH-26, SACCHAROMYCES/MAGNESIUM FERMENT, DIMETHYL ISOSORBIDE, PEG/PPG-18/18 DIMETHICONE, ETHOXYDIGLYCOL, CARNITINE HCL, ORYZA SATIVA (RICE) BRAN, PEG-40 HYDROGENATED CASTOR OIL, BIOTIN/FOLIC ACID/CYANOCOBALAMIN/NIACINAMIDE/PANTOTHENIC ACID/PYRIDOXINE/RIBOFLAVIN/THIAMINE/YEAST POLYPEPTIDES, SACCHAROMYCES/IRON FERMENT, SACCHAROMYCES/COPPER FERMENT, SACCHAROMYCES/SILICON FERMENT, SACCHAROMYCES/ZINC FERMENT, ACACIA SENEGAL GUM, UBIQUINONE.
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 200 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
NIOXIN SCALP RECOVERY MEDICATING CLEANSER
pyrithione zinc lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69282-007 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) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL ALCOHOL (UNII: 936JST6JCN) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) DIMETHICONE (UNII: 92RU3N3Y1O) GLUTAMIC ACID (UNII: 3KX376GY7L) BENZYL ALCOHOL (UNII: LKG8494WBH) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYLPARABEN (UNII: A2I8C7HI9T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PEPPERMINT OIL (UNII: AV092KU4JH) MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) GREEN TEA LEAF (UNII: W2ZU1RY8B0) PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) LEVOCARNITINE HYDROCHLORIDE (UNII: J3Y5E6IKS3) RICE BRAN (UNII: R60QEP13IC) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) ACACIA (UNII: 5C5403N26O) UBIDECARENONE (UNII: EJ27X76M46) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69282-007-50 1 in 1 CARTON 07/01/2016 1 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:69282-007-20 200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2016 3 NDC:69282-007-10 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 07/01/2016 Labeler - The Wella Corporation (001399815) Registrant - Coty US LLC (039056361) Establishment Name Address ID/FEI Business Operations Thibiant International, Inc. 118542196 manufacture(69282-007)