Home NDC 49967-899 La Roche Posay Laboratoire Dermatologique
Product NDC 49967-899
11-digit product format 499670899
Labeler code 49967
Product ID 49967-899_2af1e670-d87a-423c-a0dc-9aac07b4166a
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide
Dosage form LOTION
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-06-01
Substance TITANIUM DIOXIDE
Active strength 110 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 La Roche Posay Laboratoire Dermatologique
Brand name suffix Anthelios 50 Tinted Mineral Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 110 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP 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 49967-899-01 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Tinted Mineral Sunscreen 50 mL in 1 BOTTLE, PLASTIC LOTION 50 21 49967-899-01 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Tinted Mineral Sunscreen 1 in 1 CARTON LOTION 1 21 49967-899-02 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Tinted Mineral Sunscreen 3 mL in 1 TUBE LOTION 3 21 49967-899-02 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Tinted Mineral Sunscreen 1 in 1 CARTON LOTION 1 21 49967-899-03 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Tinted Mineral Sunscreen 1 in 1 CARTON LOTION 1 21 49967-899-03 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Tinted Mineral Sunscreen 125 mL in 1 BOTTLE LOTION 125 21
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-899 LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 TINTED MINERAL SUNSCREEN (TITANIUM DIOXIDE) LOTION [L'OREAL USA PRODUCTS INC] 21 Current NDC, Legacy NDC, 6 package rows 20240101_6d3c5fc5-c818-46c4-8db3-cffcdcd56e06.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 109 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 49967-899-01 49967089901 1 BOTTLE, PLASTIC in 1 CARTON (49967-899-01) / 50 mL in 1 BOTTLE, PLASTIC 2012-06-01 0000-00-00 No No Current 49967-899-02 49967089902 1 TUBE in 1 CARTON (49967-899-02) / 3 mL in 1 TUBE 1 tube 2012-06-01 0000-00-00 No No Current 49967-899-03 49967089903 1 BOTTLE in 1 CARTON (49967-899-03) / 125 mL in 1 BOTTLE 1 bottle 2012-06-01 0000-00-00 No No Current