NDC | 49967-052-01, 49967-052-02 |
Set ID | 8564f2cf-b680-4e2c-8451-f345c9852c1a |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART358H |
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor 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, fragrance, citric acid, sodium benzoate, sodium hydroxide, coco-betaine, carbomer, menthol, guar hydroxypropyltrimonium chloride, limonene, sodium polynaphthalenesulfonate, salicylic acid, hexyl cinnamal, coumarin, benzyl alcohol, linalool, amyl cinnamal, pentylene glycol, mentha piperita (peppermint) extract, cellulose gum, fumaric acid, methylisothiazolinone
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MATRIX BIOLAGE SCALPSYNC ANTIDANDRUFF
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-052 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) MENTHOL (UNII: L7T10EIP3A) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) LIMONENE, (+)- (UNII: GFD7C86Q1W) SALICYLIC ACID (UNII: O414PZ4LPZ) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) COUMARIN (UNII: A4VZ22K1WT) BENZYL ALCOHOL (UNII: LKG8494WBH) LINALOOL, (+/-)- (UNII: D81QY6I88E) .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418) PENTYLENE GLYCOL (UNII: 50C1307PZG) MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) FUMARIC ACID (UNII: 88XHZ13131) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-052-01 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2014 2 NDC:49967-052-02 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 05/01/2014 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, INC. 960317444 manufacture(49967-052) , pack(49967-052)