Home NDC 49967-014 CeraVe Developed with Dermatologists Sunscreen Broad Spectrum SPF 50
Product NDC 49967-014
11-digit product format 499670014
Labeler code 49967
Product ID 49967-014_ba81290e-6316-4cda-9b20-ac2c7b8ca112
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form STICK
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-11-01
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength .8; .63 g/13.32g; g/13.32g
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 CeraVe Developed with Dermatologists Sunscreen Broad Spectrum SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE .8 g/13.32g ZINC OXIDE .63 g/13.32g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII 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 49967-014-01 CeraVe Developed with Dermatologists Sunscreen Broad Spectrum SPF 50 13.32 g in 1 BLISTER PACK STICK 13.32 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-014 CERAVE DEVELOPED WITH DERMATOLOGISTS SUNSCREEN BROAD SPECTRUM SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) STICK [L'OREAL USA PRODUCTS INC] 4 Current NDC, Legacy NDC, 1 package rows 20240101_27d82e37-67ac-4cd3-83c0-fb8388d3a0dd.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49967-014-01 49967001401 13.32 g in 1 BLISTER PACK (49967-014-01) 13.32 g 2017-11-01 0000-00-00 No No Current