MATRIX BIOLAGE SCALPSYNC ANTIDANDRUFF- pyrithione zinc shampoo 
L'Oreal USA Products Inc

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.

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Drug Facts

Active ingredient

Pyrithione zinc 1%

Purpose

Antidandruff

Use

fights scalp scaling, itching and flaking due to dandruff

Warnings

For external use only

When using this product

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

condition worsens or does not improve after regular use

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

- for best results use at least twice a week or as directed by a physician

- shake well; apply evenly onto scalp

- leave on 1 - 3 minutes; rinse

- repeat if necessary

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

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MATRIX BIOLAGE SCALPSYNC ANTIDANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-052
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-052-01400 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2014
2NDC:49967-052-021000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H05/01/2014
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, INC.960317444manufacture(49967-052) , pack(49967-052)

Revised: 11/2020
 
L'Oreal USA Products Inc