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 282 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join H.E.B Solutions Sunscreen SPORT SPF 70 CONTINUOUS SPRAY H.E.B f9b5b360-6b69-4006-934f-5bc8a9fdfcd0 2024-10-15 Warnings Exact identifier application number: M020 HEB GENERAL PROTECTION SPF 100 LOTION H-E-B 39d94e3a-98c8-44b0-bd2d-f318ac7bbf75 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen WET PROTECTION KIDS SPF 70 CONTINUOUS SPRAY H.E.B f823b236-5884-41d9-bff0-65b91664aaad 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen COOLING SPORT SPF 50 CONTINUOUS SPRAY H.E.B 67fdf3a0-08fe-4348-a4f9-a83f3cf46b72 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 70 CONTINUOUS SPRAY H.E.B c16935ce-afdb-4571-b5a3-6dc5d01f721c 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen BABY SPF 50 LOTION SPRAY H.E.B 1082111f-bf04-4a98-b6a0-5da933652f1d 2024-10-15 Warnings Exact identifier application number: M020 H.E.B ULTRA SPF 50 SUNSCREEN H.E.B d6184ba2-0e47-459a-8777-1f27be2140a6 2024-10-15 Warnings Exact identifier application number: M020 H.E.B ULTRA SPF 30 SUNSCREEN H.E.B 90287874-cdfa-489c-936d-e487f6b3db96 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 2c9258ac-8cbe-4acf-9c02-bb993d69a3e5 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 39bf1379-3dee-4aa0-967a-36faccca4216 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 100 CONTINUOUS SPRAY H.E.B 301ae7e5-5a60-45d0-8cd5-553ba07db4c5 2024-10-15 Warnings Exact identifier application number: M020 Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 28C HOMOSALATE, ZINC OXIDE Rare Beauty, LLC 2470d78c-724f-4181-e063-6294a90afeaa 2024-10-14 Warnings Exact identifier application number: M020 Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 44N HOMOSALATE, ZINC OXIDE Rare Beauty, LLC 2471e0fa-ddc8-1c62-e063-6294a90a4408 2024-10-14 Warnings Exact identifier application number: M020 Walgreens 70 Hydrating Sport Broad Spectrum SPF 70 Sunscreen AVOBENZONE. HOMOSALATE, OCTISALATE, OCTOCRYLENE WALGREEN COMPANY fa2d08be-f67f-60dd-e053-6294a90adb3f 2024-10-14 Warnings Exact identifier application number: M020 Walgreens 90 Sport Continuous AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE WALGREEN COMPANY fa2e5b1b-f38f-11fe-e053-6394a90a4988 2024-10-14 Warnings Exact identifier application number: M020 Walgreens 70 Sheer Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE WALGREEN COMPANY fc635082-0a7a-f160-e053-6394a90abba3 2024-10-14 Warnings Exact identifier application number: M020 WALGREENS SPORT SPF 50 SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Walgreen Company a9ee1c60-6091-2229-e053-2995a90aa528 2024-10-14 Warnings Exact identifier application number: M020 WALGREENS BROAD SPECTRUM SPORT SPF 50 SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE WALGREEN COMPANY b10bdd6e-aa94-470f-8bbf-ff27a1d81938 2024-10-14 Warnings Exact identifier application number: M020 Walgreens Dry Touch Broad Spectrum SPF 55 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE WALGREEN COMPANY c628b15c-5fd2-fa5a-e053-2a95a90a43ac 2024-10-14 Warnings Exact identifier application number: M020 Walgreens SPF 30 Hydrating Continuous AVOBENZONE, HOMOSALATE, OCTOCRYLENE, WALGREEN COMPANY c8ae7f1a-d198-6609-e053-2a95a90ad462 2024-10-14 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