Drug Facts

Manufacturer
L'Oreal USA Products Inc. | Interspray
Effective date
2024-12-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:50:12

Label at a glance#

ProductKerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment
Active ingredientSALICYLIC ACID
Label structure10 sections

Dosage and administration

apply to affected areas one to 4 times daily or as directed by a doctor  use before going to bed for 4 weeks apply 4 doses on scalp section by section (1 dose = 1 pipette) do not rinse

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1.8%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

  • helps eliminate the symptoms of 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 of this product as directed

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

  • apply to affected areas one to 4 times daily or as directed by a doctor 
  • use before going to bed for 4 weeks
  • apply 4 doses on scalp section by section (1 dose = 1 pipette)
  • do not rinse

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol denat., aminomethyl propanol, fragrance, PEG-40 hydrogenated castor oil, bifida ferment lysate, limonene, glycerin, benzyl salicylate, benzyl alcohol, linalool, citronellol, citral, geraniol, artemisia umbelliformis flower extract, coumarin, phenoxyethanol, sodium benzoate, citric acid, potassium sorbate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2627647salicylic acid 1.8 % Topical SolutionPSN5
2627647salicylic acid 18 MG/ML Topical SolutionSCD5
2627647salicylic acid 1.8 % Topical SolutionSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-363-01Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment90 mL in 1 BOTTLELIQUID905
49967-363-01Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment1 in 1 CARTONLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49967-363KERASTASE PARIS K SYMBIOSE SERUM NUIT ANTIPELLICULAIRE INTENSIF ANTIDANDRUFF TREATMENT (SALICYLIC ACID) LIQUID [L'OREAL USA PRODUCTS INC.]5Current NDC, 2 package rows20250101_d72688ed-d153-4eed-988f-5386eb68559d.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-36349967-363-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff TreatmentSALICYLIC ACIDL'Oreal USA Products Inc.d72688ed-d153-4eed-988f-5386eb68559d2024-12-30WarningsExact identifier
ndc (package): 49967-363-01
ndc (product): 49967-363
ndc11 (package): 49967036301
spl id: 89fa668f-d2de-4e44-abb7-041277fdc741
spl set id: d72688ed-d153-4eed-988f-5386eb68559d

Reported adverse events (FAERS/openFDA)#

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