LOreal Paris Hair Expert Ever Fresh Sulfate Free Antidandruff

Manufacturer
L'Oreal USA Products Inc | L'Oreal USA, Inc.
Effective date
2023-01-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:38:59

Label at a glance#

ProductLOreal Paris Hair Expert Ever Fresh Sulfate Free Antidandruff
Active ingredientPYRITHIONE ZINC
Label structure11 sections

Dosage and administration

for best results, use at least twice a week or as directed by a doctor apply to wet hair by gently massaging onto scalp and hair rinse well

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithone zinc 1%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

helpls prevent recurrence of scalp flaking and itching associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • for best results, use at least twice a week or as directed by a doctor
  • apply to wet hair by gently massaging onto scalp and hair
  • rinse well

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, disodium laureth sulfosuccinate, sodium lauryl sulfoacetate, decyl glucoside, sodium lauroyl sarcosinate, glycol distearate, sodium chloride, coco-betaine, fragrance, amodimethicone, PPG-5-ceteth-20, acrylates copolymer, sodium benzoate, carbomer, PEG-55 propylene glycol oleate, propylene glycol, polyquaternium-39, menthol, benzoic acid, sorbitol, butylene glycol, trideceth-6, citronellol, sodium polynaphthalenesulfonate, linalool, limonene, geraniol, cetrimonium chloride, citral, cellulose gum, algae extract, melia azadirachta leaf extract, methylisothiazolinone, phenoxyethanol, potassium sorbate, sodium hydroxide, citric acid

Questions or comments?

OTC - QUESTIONS SECTION

1-800-631-7358

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-34349967-343-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

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
b59d8e85-b40d-4b7c-a525-e6645778033dbaeb3d48-483c-42e5-ad0c-21393ece45562023-01-24WarningsExact identifier
spl id: b59d8e85-b40d-4b7c-a525-e6645778033d
spl set id: baeb3d48-483c-42e5-ad0c-21393ece4556

Reported adverse events (FAERS/openFDA)#

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