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 286 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bright as Day Mineral SPF50 ZINC OXIDE Koco Life LLC 1c245a53-4098-62e6-e063-6294a90abf12 2024-09-23 Warnings Exact identifier application number: M020 Pure Protect Mineral Sunscreen Stick SPF50 ZINC OXIDE Koco Life LLC 22cd5999-9b9a-91a3-e063-6394a90a0da5 2024-09-23 Warnings Exact identifier application number: M020 ABSOLUTELY natural Lip Balm Broad Spectrum SPF 15 Sunscreen ZINC OXIDE Absolutely Natural eb914dd8-9b11-44dd-8c4f-4d4c0c3bf1ea 2024-09-23 Warnings Exact identifier application number: M020 SUNSCREEN 01 AVOBENZONE,HOMOSALATE,OCTOCRYLENE,OCTISALATE Cosmuses Cosmetics (Ningbo) Co., Ltd. 229dabbc-9043-3c9d-e063-6394a90a5692 2024-09-21 Warnings Exact identifier application number: M020 GLC OG Natural Tinted SPF 30 Sunscreen ZINC OXIDE GUD LIFE CO. LLC 25e1e8ec-e19d-45f7-b339-5d12c2b511d6 2024-09-18 Warnings Exact identifier application number: M020 Target Up and Up Sunscreen SPF 30 SPORT Broad Spectrum AVOBENZONE, HOMOSALATE,OCTISALATE,OCTOCRYLENE TARGET CORPORATION bad7d56e-662e-0776-e053-2a95a90a0af0 2024-09-18 Warnings Exact identifier application number: M020 Target Up and Up Kids SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE TARGET CORPORATION b82b6d0d-616d-f041-e053-2995a90ae6a3 2024-09-18 Warnings Exact identifier application number: M020 COOLA Dew Good Illuminating Body Melt SPF 40 AVOBENZONE, OCTISALATE, OCTOCRYLENE COOLA LLC 43d293f6-e13c-4ee9-89df-2a3ef0034e31 2024-09-16 Warnings Exact identifier application number: M020 Proceuticals Private Label by TiZO non-tinted replenishing daily protection ZINC OXIDE Fallien Cosmeceuticals, Ltd 2203ea22-d12a-99fe-e063-6394a90aca9f 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Tinted ZINC OXIDE Allure Labs 22042031-ac8e-1ab2-e063-6394a90a6ed4 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Tinted ZINC OXIDE ONESKIN INC. 2204e776-b1a1-be15-e063-6294a90af5de 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Untinted ZINC OXIDE Allure Labs 2205345b-5e92-37eb-e063-6294a90a6b6c 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Untinted ZINC OXIDE ONESKIN INC. 2205ec0e-ac3f-299f-e063-6294a90a2174 2024-09-13 Warnings Exact identifier application number: M020 H-E-B SOLUTIONS SUNSCREEN COCONUT SPF 50 CONTINUOUS AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B f4130277-ea9b-6b25-e053-2a95a90a59be 2024-09-13 Warnings Exact identifier application number: M020 HEB SPF 50 Tattoo Continuous Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B f6df491d-1fa9-a4c8-e053-6394a90a3866 2024-09-13 Warnings Exact identifier application number: M020 YOUR Day Cream Sunscreen Broad Spectrum SPF 30 OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE Skin Ai, LLC 21cbd5ac-5307-939b-e063-6294a90ac791 2024-09-10 Warnings Exact identifier application number: M020 Mario Badescu SPF 17 AVOBENZONE, OCTINOXATE, OCTOCRYLENE Bentley Laboratories LLC 0fd51f8d-ee67-48fd-ab98-1fedb0339462 2024-09-10 Warnings Exact identifier application number: M020 Mario Badescu Collagen SPF 15 AVOBENZONE, OCTINOXATE, OXYBENZONE Bentley Laboratories LLC 0246b11b-f1ba-4f47-91ab-52a6554b9467 2024-09-10 Warnings Exact identifier application number: M020 Mario Badescu The Moisture Magnet SPF 15 AVOBENZONE, OCTINOXATE, OXYBENZONE Bentley Laboratories LLC f6d653f5-52a0-42ad-8308-b8d6f57050cc 2024-09-10 Warnings Exact identifier application number: M020 MARIO BADESCU SPF 30 AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Bentley Laboratories LLC fe485d4c-0ded-4061-ac34-77b72d535090 2024-09-10 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