Home NDC 49967-900 CeraVe Developed with Dermatologists Skin Renewing Broad Spectrum SPF 30 Day
Product NDC 49967-900
11-digit product format 499670900
Labeler code 49967
Product ID 49967-900_246b0293-ab86-44b4-b615-fef215ef0ce7
Type HUMAN OTC DRUG
Nonproprietary name octinoxate and zinc oxide
Dosage form CREAM
Route TOPICAL
Labeler L'Oreal USA Products Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-08-28
Substance OCTINOXATE; ZINC OXIDE
Active strength 75; 105 mg/g; mg/g
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 Skin Renewing Broad Spectrum SPF 30 Day
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 75 mg/g ZINC OXIDE 105 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 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 49967-900-01 CeraVe Developed with Dermatologists Skin Renewing Broad Spectrum SPF 30 Day 1 in 1 CARTON CREAM 1 4 49967-900-01 CeraVe Developed with Dermatologists Skin Renewing Broad Spectrum SPF 30 Day 50 g in 1 BOTTLE, PUMP CREAM 50 4 49967-900-02 CeraVe Developed with Dermatologists Skin Renewing Broad Spectrum SPF 30 Day 5 g in 1 TUBE CREAM 5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-900 CERAVE DEVELOPED WITH DERMATOLOGISTS SKIN RENEWING BROAD SPECTRUM SPF 30 DAY (OCTINOXATE AND ZINC OXIDE) CREAM [L'OREAL USA PRODUCTS INC.] 4 Current NDC, Legacy NDC, 3 package rows 20240101_50542a3b-2ef0-452f-b463-79b41e10d1e0.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 49967-900-01 49967090001 1 BOTTLE, PUMP in 1 CARTON (49967-900-01) / 50 g in 1 BOTTLE, PUMP 2017-08-28 0000-00-00 No No Current 49967-900-02 49967090002 5 g in 1 TUBE (49967-900-02) 5 g 2017-08-28 0000-00-00 No No Current