LOreal Professionnel Paris

Manufacturer
L'Oreal Productos Capilares
Effective date
2011-03-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:51:38

Label at a glance#

ProductLOreal Professionnel Paris Instant Clear Antidandruff
Active ingredientPyrithione Zinc
Label structure11 sections

Indications and uses

helps prevent recurrence of the symptoms of dandruff helps eliminate scalp flaking and itching associated with dandruff

Dosage and administration

for best results, use at least twice a week or as directed by a physician shake well wet hair and apply a small amount of shampoo massage vigorously rinse well repeat if necessary

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 1%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Uses

INDICATIONS & USAGE SECTION

  • helps prevent recurrence of the symptoms of dandruff
  • helps eliminate scalp flaking and itching associated with dandruff

Directions

DOSAGE & ADMINISTRATION SECTION

  • for best results, use at least twice a week or as directed by a physician
  • shake well
  • wet hair and apply a small amount of shampoo
  • massage vigorously
  • rinse well
  • repeat if necessary

Warnings

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if

condition worsens or does not improve after regular use

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

OTC - WHEN USING SECTION

When using this product

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

Warnings

OTC - STOP USE SECTION

Stop use and ask a doctor if

condition worsens or does not improve after regular use

Warnings

WARNINGS SECTION

For external use only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Since not required by regulation, intentionally omitted.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43325-828-012020-01-25C16284748780-1960f7f55-cfd1-8e05-e053-dbdaa90a074aDrug Facts
43325-828-012019-10-29C16284748780-1960f7f55-cfd1-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Pyrithione ZincACTIVE INGREDIENTR953O2RHZ52
Pyrithione ZincACTIVE MOIETYR953O2RHZ52

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43325-82843325-828-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Pyrithione ZincR953O2RHZ5ACTIB

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
3813c8fa-00d6-483a-98a9-c6a98aa683b33693588f-4fa0-4fa0-a895-5c0d189a74ec2020-01-24WarningsExact identifier
spl set id: 3693588f-4fa0-4fa0-a895-5c0d189a74ec

Reported adverse events (FAERS/openFDA)#

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