REDKEN 5TH AVENUE NYC SCALP RELIEF DANDRUFF CONTROL- pyrithione zinc shampoo 
L'Oreal USA Products Inc

----------

Drug Facts

Active ingredient

Pyrithione zinc 1%

Purpose

Antidandruff

Uses

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 physician 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

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

image of front label

image of front label

image description
REDKEN 5TH AVENUE NYC SCALP RELIEF DANDRUFF CONTROL 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-795
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)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-795-01300 mL in 1 BOTTLE; Type 0: Not a Combination Product08/17/200608/01/2022
2NDC:49967-795-02250 mL in 1 BOTTLE; Type 0: Not a Combination Product10/13/202012/30/2021
3NDC:49967-795-03250 mL in 1 TUBE; Type 0: Not a Combination Product10/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03208/17/2006
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'OREAL USA, INC.960317444manufacture(49967-795)

Revised: 12/2023
Document Id: 099d44dc-eff9-47d9-b252-e9f633f0016b
Set id: 306a1ef4-e7ed-4c8c-877c-3c34d3e6d7b7
Version: 9
Effective Time: 20231211
 
L'Oreal USA Products Inc