Home NDC 49967-907 La Roche Posay Laboratoire Dermatologique
Product NDC 49967-907
11-digit product format 499670907
Labeler code 49967
Product ID 49967-907_93f2cacd-67af-4ad8-9e0a-4de8330f808f
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 2011-07-01
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 60; 50 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Mineral Ultra Light Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 60 mg/mL ZINC OXIDE 50 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 49967-907-01 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen 50 mL in 1 BOTTLE, PLASTIC LOTION 50 17 49967-907-01 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen 1 in 1 CARTON LOTION 1 17 49967-907-02 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen 3 mL in 1 TUBE LOTION 3 17 49967-907-02 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen 1 in 1 CARTON LOTION 1 17 49967-907-03 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen 5 mL in 1 TUBE LOTION 5 17 49967-907-03 La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen 1 in 1 CARTON LOTION 1 17
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-907 LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC] 17 Current NDC, Legacy NDC, 6 package rows 20231214_2ce83dc2-84b6-43fd-8b11-495d41cebc22.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 178 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sunforgettable Total Protection Sport Stick ZINC OXIDE Colorescience d3c0d2b0-f411-565d-e053-2a95a90a081b 2025-10-15 Warnings Exact identifier application number: M020 Defend and Balance TInted Mineral Sunscreen SPF 50 SUNSCREEN Epicuren Discovery 41367f05-59d8-6736-e063-6394a90a5f17 2025-10-15 Warnings Exact identifier application number: M020 Banana Boat AVOBENZONE HOMOSALATE OCTOCRYLENE Edgewell Personal Care Brands LLC 41376da3-5274-b133-e063-6394a90afa13 2025-10-15 Warnings Exact identifier application number: M020 Curology Daily Moisturizing Sunscreen SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Curology ee59d52e-5dc6-4fb4-96d8-0bda40e23009 2025-10-15 Warnings Exact identifier application number: M020 SUNFORGETTABLE TOTAL PROTECTION COLOR BALM COLLECTION ENDLESSS ENDLESS SUNSET ZINC OXIDE Colorescience f4aa14ed-6c6f-8301-e053-2a95a90a5e23 2025-10-15 Warnings Exact identifier application number: M020 Curology The Lip Balm Broad Spectrum SPF 30 Sunscreen ZINC OXIDE Curology Inc. e441b13f-cb58-457f-e053-2a95a90adab9 2025-10-15 Warnings Exact identifier application number: M020 Curology Everyday Sunscreen Broad Spectrum SPF 30 No-clog UV defense ZINC OXIDE Curology 39a2a297-3af2-40d3-8b5d-f4eef2487fb2 2025-10-15 Warnings Exact identifier application number: M020 Colorescience Total Protection No Show Mineral Sunscreen ZINC OXIDE Colorescience 00d8bf32-aecd-22da-e063-6294a90a7567 2025-10-15 Warnings Exact identifier application number: M020 Impeccable Skin Sunscreen Foundation Broad Spectrum SPF 30 Sand ZINC OXIDE Cosmetic Enterprises Ltd 253c105b-215b-1e6e-e063-6294a90a11d7 2025-10-14 Warnings Exact identifier application number: M020 Impeccable Skin Sunscreen Foundation Broad Spectrum SPF 30 Tan ZINC OXIDE Cosmetic Enterprises Ltd 265bbb1a-ba96-6598-e063-6394a90a9415 2025-10-14 Warnings Exact identifier application number: M020 Resist Wrinkle Defense SPF 30 Paulas Choice ZINC OXIDE Cosmetic Enterprises Ltd d658fdc7-9dac-47bf-8e83-1433a29a6cf6 2025-10-14 Warnings Exact identifier application number: M020 SPF 50 Face Sunscreen Bioelements AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE Cosmetic Enterprises Ltd 498b16c8-ba54-4a0a-8dbc-4b5cc368e214 2025-10-14 Warnings Exact identifier application number: M020 Skin Balancing Ultra Sheer Daily Defence SPF 30 Paulas Choice AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OXYBENZONE Cosmetic Enterprises Ltd 3bf31626-5580-457b-8a59-cc37f4ab0767 2025-10-14 Warnings Exact identifier application number: M020 Sunscreen Broad Spectrum SPF 30 Light Tropical Scent ZINC OXIDE Cosmetic Enterprises Ltd d8c7b82d-6151-2199-e053-2a95a90a6c20 2025-10-14 Warnings Exact identifier application number: M020 TOCOBO Cotton Airy Sun Stick AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE PICTON CO., Ltd. 412975d8-0b8b-23bf-e063-6294a90a5568 2025-10-14 Warnings Exact identifier application number: M020 TOCOBO Bio Watery Sun Screen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE PICTON CO., Ltd. 4129e00b-951d-adbf-e063-6294a90a675e 2025-10-14 Warnings Exact identifier application number: M020 Sunny Sailor First Mate Face Stick SPF 30 ZINC OXIDE SUNNY SAILOR LLC c7908385-ff93-4c6c-9462-081c73023571 2025-10-13 Warnings Exact identifier application number: M020 Cloud Brush On Sunscreen SPF 50 ZINC OXIDE FUTURE 8 LLC 8b1eaf6c-9cd8-4c5e-beac-b8539c332ae3 2025-10-13 Warnings Exact identifier application number: M020 Sunplus Mist Sunscreen SPF 30 AVOBENZONE, OCTISALATE, OCTOCRYLENE SUNPLUS SKIN CARE LLC 951a7bdc-d5c5-4241-a482-c30a4b44f776 2025-10-13 Warnings Exact identifier application number: M020 Sunplus Mist Sunscreen SPF 50 AVOBENZONE, OCTISALATE, OCTOCRYLENE SUNPLUS SKIN CARE LLC da338ba7-7a92-4157-97f4-5ae9cc64853c 2025-10-13 Warnings Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49967-907-01 49967090701 1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01) / 50 mL in 1 BOTTLE, PLASTIC 2011-07-01 0000-00-00 No No Current 49967-907-02 49967090702 1 TUBE in 1 CARTON (49967-907-02) > 3 mL in 1 TUBE 1 tube 2011-07-01 0000-00-00 No No Current 49967-907-03 49967090703 1 TUBE in 1 CARTON (49967-907-03) / 5 mL in 1 TUBE 1 tube 2019-12-02 0000-00-00 No No Current