MIZANI SCALP CARE CONDITIONER ANTIDANDRUFF CONDITIONER- pyrithione zinc lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient

Pyrithione zinc 1%

Purpose

Antidandruff

Use

helps eliminate recurrence of scalp flaking, scaling, and itching associated with dandruff

Warnings

For external use only


When using this product 

do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and consult 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, cetearyl alcohol, behentrimonium chloride, glycerin, PEG-180, amodimethicone, cetyl esters, isopropyl alcohol, fragrance, methylparaben, hydroxyethylcellulose, menthol, trideceth-6, benzyl benzoate, propylene glycol, benzyl alcohol, sodium polynaphthalenesulfonate, benzyl salicylate, chlorhexidine dihydrochloride, citronellol, cetrimonium chloride, geraniol, mentha piperita (peppermint) oil, alpha-isomethyl ionone, cellulose gum, cucumis sativus (cucumber) fruit extract, methylisothiazolinone

image of a label

image of a label
MIZANI SCALP CARE CONDITIONER ANTIDANDRUFF CONDITIONER 
pyrithione zinc lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-389
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)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
AMODIMETHICONE (1300 CST) (UNII: 3V7U636DWN)  
CETYL ESTERS WAX (UNII: D072FFP9GU)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
MENTHOL (UNII: L7T10EIP3A)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
BENZYL BENZOATE (UNII: N863NB338G)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
CHLORHEXIDINE HYDROCHLORIDE (UNII: E64XL9U38K)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-389-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2008
2NDC:49967-389-021000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03206/01/2008
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.960317444manufacture(49967-389)

Revised: 12/2023
Document Id: 007e125f-8b6b-4791-8250-70064d9385b3
Set id: d337e40d-a066-4bab-8da8-b53fca29962f
Version: 9
Effective Time: 20231211
 
L'Oreal USA Products Inc