Home NDC 49967-242 CeraVe Anti-Dandruff Hydrating Conditioner
Product NDC 49967-242
11-digit product format 499670242
Labeler code 49967
Product ID 49967-242_cb2a5460-c548-4ead-855e-5ff29a17ee37
Type HUMAN OTC DRUG
Nonproprietary name Pyrithione Zinc
Dosage form LIQUID
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-01
Substance PYRITHIONE ZINC
Active strength 5 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 CeraVe Anti-Dandruff Hydrating Conditioner
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PYRITHIONE ZINC 5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R953O2RHZ5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1043014 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-242-01 CeraVe Anti-Dandruff Hydrating Conditioner 266 mL in 1 TUBE LIQUID 266 2 49967-242-02 CeraVe Anti-Dandruff Hydrating Conditioner 26 mL in 1 PACKET LIQUID 26 2 49967-242-03 CeraVe Anti-Dandruff Hydrating Conditioner 15 in 1 PACKAGE LIQUID 15 2 49967-242-03 CeraVe Anti-Dandruff Hydrating Conditioner 29 mL in 1 TUBE LIQUID 29 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-242 CERAVE ANTI-DANDRUFF HYDRATING CONDITIONER (PYRITHIONE ZINC) LIQUID [L'OREAL USA PRODUCTS INC] 1 Current NDC, 4 package rows 20241225_d6a704df-edd8-4960-a088-246519e2aecf.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 15 of 31 · 615 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 49967-242-01 49967024201 266 mL in 1 TUBE (49967-242-01) 266 ml 2024-11-01 No No Current 49967-242-02 49967024202 26 mL in 1 PACKET (49967-242-02) 26 ml 2024-11-01 No No Current 49967-242-03 49967024203 15 TUBE in 1 PACKAGE (49967-242-03) / 29 mL in 1 TUBE 15 tube 2026-05-12 No No Current