Label: MIZANI SCALP CARE ANTIDANDRUFF- pyrithione zinc shampoo
- NDC Code(s): 49967-388-01, 49967-388-02
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2023
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- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and consult a physician if
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, sodium laureth sulfate, sodium lauryl sulfate, coco-betaine, glycol distearate, dimethicone, sodium chloride, glycerin, disodium cocoamphodiacetate, fragrance, sodium benzoate, sodium hydroxide, citric acid, polyquaternium-10, methylparaben, cocamide MIPA, carbomer, salicylic acid, menthol, ethylparaben, benzyl benzoate, propylene glycol, benzyl alcohol, sodium polynaphthalenesulfonate, benzyl salicylate, citronellol, geraniol, mentha piperita (peppermint) oil, alpha-isomethyl ionone, cellulose gum, cucumis sativus (cucumber) fruit extract, methylisothiazolinone
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INGREDIENTS AND APPEARANCE
MIZANI SCALP CARE ANTIDANDRUFF
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-388 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) COCO-BETAINE (UNII: 03DH2IZ3FY) GLYCOL DISTEARATE (UNII: 13W7MDN21W) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM CHLORIDE (UNII: 451W47IQ8X) GLYCERIN (UNII: PDC6A3C0OX) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK) METHYLPARABEN (UNII: A2I8C7HI9T) COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) SALICYLIC ACID (UNII: O414PZ4LPZ) MENTHOL (UNII: L7T10EIP3A) ETHYLPARABEN (UNII: 14255EXE39) BENZYL BENZOATE (UNII: N863NB338G) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZYL ALCOHOL (UNII: LKG8494WBH) BENZYL SALICYLATE (UNII: WAO5MNK9TU) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) GERANIOL (UNII: L837108USY) PEPPERMINT OIL (UNII: AV092KU4JH) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) CUCUMBER (UNII: YY7C30VXJT) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-388-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2008 2 NDC:49967-388-02 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 06/01/2008 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 960317444 manufacture(49967-388)