Home NDC 49967-363 Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment
Product NDC 49967-363
11-digit product format 499670363
Labeler code 49967
Product ID 49967-363_89fa668f-d2de-4e44-abb7-041277fdc741
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form LIQUID
Route TOPICAL
Labeler L'Oreal USA Products Inc.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-12-01
Substance SALICYLIC ACID
Active strength 18 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 18 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2627647 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-363-01 Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment 90 mL in 1 BOTTLE LIQUID 90 5 49967-363-01 Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment 1 in 1 CARTON LIQUID 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-363 KERASTASE PARIS K SYMBIOSE SERUM NUIT ANTIPELLICULAIRE INTENSIF ANTIDANDRUFF TREATMENT (SALICYLIC ACID) LIQUID [L'OREAL USA PRODUCTS INC.] 5 Current NDC, 2 package rows 20250101_d72688ed-d153-4eed-988f-5386eb68559d.zip
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 13 of 31 · 613 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 49967-363-01 49967036301 1 BOTTLE in 1 CARTON (49967-363-01) / 90 mL in 1 BOTTLE 1 bottle 2022-12-01 No No Current