NDC | 49967-795-01 |
Set ID | 306a1ef4-e7ed-4c8c-877c-3c34d3e6d7b7 |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART358H |
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a physician if
- Keep out of reach of children.
- Directions
-
Inactive ingredients
water, sodium laureth sulfate, sodium lauryl sulfate, glycerin, cocamide MEA, glycol distearate, sodium chloride, hexylene glycol, dimethicone, citric acid, fragrance, sodium benzoate, sodium hydroxide, coco-betaine, carbomer, guar hydroxypropyltrimonium chloride, menthoxypropanediol, sodium polynaphthalenesulfonate, salicylic acid, hydrolyzed soy protein, eugenol, limonene, cellulose gum, lecithin, fumaric acid, phosphoric acid, lavandula angustifolia (lavender) oil, methylisothiazolinone, tocopherol
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
REDKEN 5TH AVENUE NYC SCALP RELIEF DANDRUFF CONTROL
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-795 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) GLYCERIN (UNII: PDC6A3C0OX) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CHLORIDE (UNII: 451W47IQ8X) HEXYLENE GLYCOL (UNII: KEH0A3F75J) DIMETHICONE (UNII: 92RU3N3Y1O) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCO-BETAINE (UNII: 03DH2IZ3FY) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH) SALICYLIC ACID (UNII: O414PZ4LPZ) HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6) EUGENOL (UNII: 3T8H1794QW) LIMONENE, (+)- (UNII: GFD7C86Q1W) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) FUMARIC ACID (UNII: 88XHZ13131) PHOSPHORIC ACID (UNII: E4GA8884NN) LAVENDER OIL (UNII: ZBP1YXW0H8) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-795-01 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/17/2006 08/01/2022 2 NDC:49967-795-02 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 08/17/2006 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC. 960317444 manufacture(49967-795) , pack(49967-795)