Home NDC 49967-589 CERAVE Hydrating Mineral Sunscreen Light Sheer Tint Broad Spectrum SPF 30
Product NDC 49967-589
11-digit product format 499670589
Labeler code 49967
Product ID 49967-589_f237d15f-c80c-464d-bbcc-ca7145ff1816
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide and Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler L�Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-08-15
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 55; 100 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Hydrating Mineral Sunscreen Light Sheer Tint Broad Spectrum SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 55 mg/mL ZINC OXIDE 100 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 49967-589-01 CERAVE Hydrating Mineral Sunscreen Light Sheer Tint Broad Spectrum SPF 30 50 mL in 1 TUBE LOTION 50 2 49967-589-01 CERAVE Hydrating Mineral Sunscreen Light Sheer Tint Broad Spectrum SPF 30 1 in 1 CARTON LOTION 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-589 CERAVE HYDRATING MINERAL SUNSCREEN LIGHT SHEER TINT BROAD SPECTRUM SPF 30 (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L’OREAL USA PRODUCTS INC] 2 Current NDC, 2 package rows 20241225_8b298516-70df-47ab-834f-51dcde28a43a.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 Sample Exclude flag Status 49967-589-01 49967058901 1 TUBE in 1 CARTON (49967-589-01) / 50 mL in 1 TUBE 1 tube 2024-08-15 No No Current