FDA.reportPublic FDA data

LOreal Paris Men Expert Antidandruff Conditioner and

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC.
Effective date
2024-06-24
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:00:11

Label at a glance#

ProductLOreal Paris Men Expert Antidandruff Conditioner and
Active ingredientPYRITHIONE ZINC
Label structure5 sections

Dosage and administration

Apply evenly to scalp, leave on for several minutes, and then rinse off. Use at least twice per week or as directed by a doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 1%

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Consult a doctor if condition worsens or does not improve after regular use of this product and prior to use for children under 2 years of age.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply evenly to scalp, leave on for several minutes, and then rinse off. Use at least twice per week or as directed by a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium laureth sulfate, coco-betaine, dimethicone, sodium chloride, glycerin, glycol distearate, acrylayes/vinyl neodecanoate crosspolymer, sodium benzoate, cocamide MIPA, polyqaternium-10, salicylic acid, aloe barbadensis leaf juice, sodium hydroxide, butylphenyl methylpropional, linalool, citronellol, geraniol, benzyl alcohol, methyl cocoate, sodium cocoate, citric acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a cartonimage of a cartonimage of a cartonimage of a carton

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49967-672LOREAL PARIS MEN EXPERT ANTIDANDRUFF CONDITIONER AND (PYRITHIONE ZINC) SHAMPOO [L'OREAL USA PRODUCTS INC]6Unmatched20240625_2456715c-ae1c-4f6f-b1af-ed2a531f3327.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-67249967-672-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
PYRITHIONE ZINCR953O2RHZ5ACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCO-BETAINE03DH2IZ3FYIACT
DIMETHICONE92RU3N3Y1OIACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCERINPDC6A3C0OXIACT
GLYCOL DISTEARATE13W7MDN21WIACT
SODIUM BENZOATEOJ245FE5EUIACT
COCO MONOISOPROPANOLAMIDE21X4Y0VTB1IACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
SALICYLIC ACIDO414PZ4LPZIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM HYDROXIDE55X04QC32IIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
LINALOOL, (+/-)-D81QY6I88EIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
GERANIOLL837108USYIACT
BENZYL ALCOHOLLKG8494WBHIACT
METHYL COCOATE92396UOJ5ZIACT
SODIUM COCOATER1TQH25F4IIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d59dd6d2-af37-42f3-ab82-997051ca598a2456715c-ae1c-4f6f-b1af-ed2a531f33272024-06-24WarningsExact identifier
spl id: d59dd6d2-af37-42f3-ab82-997051ca598a
spl set id: 2456715c-ae1c-4f6f-b1af-ed2a531f3327

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.