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 116 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETIC ACADEMY LLC 36c043e0-fd6c-5f7a-e063-6294a90a8899 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETIC ACADEMY LLC 36c0c1ca-80a8-9d37-e063-6294a90a824f 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETIC ACADEMY LLC 36c0f5df-6bfb-3c0d-e063-6294a90a2e5f 2025-12-16 Exact identifier application number: M020 Daily Protect Mineral Sunscreen ZINC OXIDE SARAH'S 4617beb7-381e-8994-e063-6394a90a14b5 2025-12-16 Warnings Exact identifier application number: M020 SHISEIDO URBAN ENVIRONMENT ENSULIZOLE, HOMOSALATE, OCTISALATE, ZINC OXIDE Shiseido Americas Corporation 8db9f5e0-a8d6-4872-b4c6-cb92c43d25c2 2025-12-16 Warnings Exact identifier application number: M020 cle de peau BEAUTE UV PROTECTIVE N AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Shiseido Americas Corporation 18ed9b7f-bdbe-45d7-a38c-6d065080ae99 2025-12-16 Warnings Exact identifier application number: M020 cle de peau BEAUTE UV PROTECTIVE FOR BODY N ENSULIZOLE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE Shiseido Americas Corporation a2bbf6f8-b8ad-4cd9-abeb-7ec0a4ddb45c 2025-12-16 Warnings Exact identifier application number: M020 b.tan Beach Please SPF 7 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Marque of Brands Americas, LLC bdc07d83-a34f-5262-e053-2995a90acfc3 2025-12-16 Warnings Exact identifier application number: M020 Daily Protect Tinted Mineral Sunscreen ZINC OXIDE SARAH'S 461910bd-1f74-f99e-e063-6394a90ae30e 2025-12-16 Warnings Exact identifier application number: M020 Daily Protect Tinted Mineral Sunscreen ZINC OXIDE SARAH'S 4619b08f-3e63-25aa-e063-6294a90a78d7 2025-12-16 Warnings Exact identifier application number: M020 meg ALL DAY SOOTHE SUN SHIELD BROAD SPECTRUM SPF48 Meg Cosmetics Inc 4526bacf-6451-b297-e063-6294a90af71a 2025-12-16 Warnings Exact identifier application number: M020 Total Eye 3-In-1 Renewal Therapy SPF 35 TITANIUM DIOXIDE AND ZINC OXIDE Colorescience 4b116cc4-94d2-4bfc-b7f9-5f486a194c6c 2025-12-16 Warnings Exact identifier application number: M020 Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32 ZINC OXIDE Onekind.25 c11197f4-cee0-04b3-e053-2995a90a1ba8 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Medium Deep ZINC OXIDE Crunchi, LLC. 69618265-2ebb-4cdc-a28f-e36c07fe5b8f 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Medium ZINC OXIDE Crunchi, LLC. 23248bc3-1b82-443a-b38a-df7f0efb5d2a 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Light ZINC OXIDE Crunchi, LLC. cf4039f5-00ee-4227-a3dc-61995c800135 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Body Sunscreen SPF 30 ZINC OXIDE Crunchi, LLC. 227f5a41-8c3c-492d-947f-e2b046208bca 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Light Medium ZINC OXIDE Crunchi, LLC. 5b3f2766-065b-4817-a5ff-bd1c7882bfc9 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Daily Facial Sunscreen SPF 30 ZINC OXIDE Cruchi, LLC. 4f3bcfa0-e43e-4284-afaa-6488ddd749f0 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3543a22c-34d5-e572-e063-6394a90ad579 2025-12-15 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