Dercos Salicylic Acid Anti-Dandruff Serum

Manufacturer
L'Oreal USA Products Inc | PRODUCTOS CAPILARES L'OREAL SA
Effective date
2024-11-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:35:40

Label at a glance#

ProductDercos Salicylic Acid Anti-Dandruff Serum
Active ingredientSALICYLIC ACID
Label structure11 sections

Indications and uses

controls the symptoms of dandruff fights recurrence of the symptoms of dandruff controls scalp itching associated with dandruff

Dosage and administration

part dry or damp hair in 4 sections apply 5 doses to each section massage product into scalp apply to affected areas one to four times daily or as directed by a doctor 

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1.85%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Uses

INDICATIONS & USAGE SECTION

  • controls the symptoms of dandruff
  • fights recurrence of the symptoms of dandruff
  • controls scalp 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 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

  • part dry or damp hair in 4 sections
  • apply 5 doses to each section
  • massage product into scalp
  • apply to affected areas one to four times daily or as directed by a doctor 

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol denat., aminomethyl propanol, ascorbyl glucoside, madecassoside, niacinamide, PEG-40 hydrogenated castor oil, polysorbate 21, sodium hyaluronate, fragrance

Questions or comments?

OTC - QUESTIONS SECTION

1-877-378-4249

Monday-Friday (9 a.m. - 5 p.m. EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2697740salicylic acid 1.85 % Topical SolutionPSN2
2697740salicylic acid 18.5 MG/ML Topical SolutionSCD2
2697740salicylic acid 1.85 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-892-01Dercos Salicylic Acid Anti-Dandruff Serum90 mL in 1 BOTTLE, PLASTICLIQUID902
49967-892-01Dercos Salicylic Acid Anti-Dandruff Serum1 in 1 CARTONLIQUID12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49967-892DERCOS SALICYLIC ACID ANTI-DANDRUFF SERUM (SALICYLIC ACID) LIQUID [L'OREAL USA PRODUCTS INC]2Current NDC, 2 package rows20241109_79a5f545-b3be-4bc3-9fc9-d2346ef17a1b.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-89249967-892-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Dercos Salicylic Acid Anti-Dandruff SerumSALICYLIC ACIDL'Oreal USA Products Inc79a5f545-b3be-4bc3-9fc9-d2346ef17a1b2024-11-07WarningsExact identifier
ndc (package): 49967-892-01
ndc (product): 49967-892
ndc11 (package): 49967089201
spl id: 883b90f5-f1bb-4399-9aee-d4d168afd000
spl set id: 79a5f545-b3be-4bc3-9fc9-d2346ef17a1b

Reported adverse events (FAERS/openFDA)#

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