Home NDC 49967-472 SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen
Product NDC 49967-472
11-digit product format 499670472
Labeler code 49967
Product ID 49967-472_fb7295ff-7c8f-4fde-951d-90b68f53e43c
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide and Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-01-01
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 50; 40 mg/mL; 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 SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 50 mg/mL ZINC OXIDE 40 mg/mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-472-01 SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen 1 in 1 CARTON CREAM 1 8 49967-472-01 SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen 50 mL in 1 BOTTLE CREAM 50 8 49967-472-02 SkinCeuticals Physical UV Defense Broad Spectrum SPF 30 Sunscreen 4 mL in 1 TUBE CREAM 4 8
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-472 SKINCEUTICALS PHYSICAL UV DEFENSE BROAD SPECTRUM SPF 30 SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [L'OREAL USA PRODUCTS INC] 8 Current NDC, Legacy NDC, 3 package rows 20250101_3a6db7d3-6c59-4633-a97e-1c03127246d3.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 162 of 353 · 7,041 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 49967-472-01 49967047201 1 BOTTLE in 1 CARTON (49967-472-01) / 50 mL in 1 BOTTLE 1 bottle 2012-01-01 0000-00-00 No No Current 49967-472-02 49967047202 4 mL in 1 TUBE (49967-472-02) 4 ml 2012-01-01 0000-00-00 No No Current