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 233 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Zealios SPF LipGuard OCTISALATE AND AVOBENZONE Personal Best Products Inc. dba Zealios 3a07822b-a7c9-40af-a8f7-bea591c7a49b 2025-01-13 Warnings Exact identifier application number: M020 SPF-30 BB ZINC OXIDE ZION HEALTH 66d33d8c-8900-4698-98fe-0dedafe674d8 2025-01-13 Warnings Exact identifier application number: M020 Priia Tinted Mineral Sunscreen and Primer TITANIUM DIOXIDE, ZINC OXIDE Priia Cosmetics Inc b2addf27-9139-48b4-85e6-618f4b5311cc 2025-01-13 Warnings Exact identifier application number: M020 Skin Apeel Ageless Defense SPF 40 Broad Spectrum ZINC OXIDE Skin Apeel, Inc. c3bbe779-b012-4f19-8b90-2c7a4dd88617 2025-01-13 Warnings Exact identifier application number: M020 UNCOMPLIKATED MAKEUP SETTING SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE KATE SOMERVILLE SKINCARE LLC 1a33cb41-440a-41cb-9832-24255bfa2b7c 2025-01-12 Warnings Exact identifier application number: M020 ALLSWELL MINERAL SUNSCREEN SPF 30 ZINC OXIDE Stream2Sea, LLC 03bee988-d6e3-4290-a926-9c5366649cba 2025-01-12 Warnings Exact identifier application number: M020 Baby Donna SHeer SPF Sunscreen Stick ZINC OXIDE Stream2Sea, LLC a1b1cdeb-e5fe-4ba1-8bb0-3c7a97dd93fe 2025-01-12 Warnings Exact identifier application number: M020 SUN PROTECT LIP BALM SPF 30 ZINC OXIDE AND TITANIUM DIOXIDE Stream2Sea, LLC 21386652-b952-48be-b077-1acecc7f0eb0 2025-01-12 Warnings Exact identifier application number: M020 Bondi Sands SPF 60 Sunny Body AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE BONDI SANDS (USA) INC. 2b5aebed-49f6-7bb8-e063-6294a90a8521 2025-01-10 Warnings Exact identifier application number: M020 Bondi Sands SPF 60 Sunny Drops Face Serum AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE BONDI SANDS (USA) INC. 2b5c69e4-2819-94ef-e063-6394a90a68e7 2025-01-10 Warnings Exact identifier application number: M020 Dermaroller Anhydrous Sunscreen SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Owen Biosciences, Inc. 04e82f1b-c893-4795-b7a9-0523e3ec7552 2025-01-10 Warnings Exact identifier application number: M020 Skinfuse Shield SPF 30 ZINC OXIDE Owen Biosciences, Inc. b8e4c11a-4b4f-4e36-a75e-0a73913113d5 2025-01-10 Warnings Exact identifier application number: M020 Correct and Protect Serum Broad Spectrum SPF 45 ZINC OXIDE Murad, LLC 60c62108-6806-4722-a44b-f1c300d59c1e 2025-01-10 Warnings Exact identifier application number: M020 Multi Vitamin Clear Coat Broad Spectrum SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Murad, LLC e023c874-c89d-4bd0-a0b9-a8161c261457 2025-01-10 Warnings Exact identifier application number: M020 CoTZ Baby ZINC OXIDE Fallien Cosmeceuticals, LTD 17cc12c7-5af8-413f-b205-31ac150583e2 2025-01-09 Warnings Exact identifier application number: M020 ISNTREE HYALURONIC ACID DAILY SUNGEL AVOBENZONE, HOMOSALATE, OCTISALATE ISNTREE Inc. 2b3bdbe1-ede9-cd60-e063-6394a90ab2f3 2025-01-09 Warnings Exact identifier application number: M020 JAFRA ROYAL REVITALIZE 4 TUBE SET AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Distribuidora Comercial Jafra, S.A. de C.V. b4a0d6ab-50a7-43e7-9d7e-a4c01d7eca98 2025-01-09 Warnings Exact identifier application number: M020 glo SKIN BEAUTY Moisturizing Tint SPF 30 GLO SKIN BEAUTY MOISTURIZING TINT SPF 30 Hayden Caleel LLC 2b464a70-8f40-3148-e063-6394a90ac18c 2025-01-09 Warnings Exact identifier application number: M020 Sunscreen and insect repellent Bull frog SPF 50 Bullfrog Brands, LLC d65d15a6-0a32-1203-e053-2995a90aa6c5 2025-01-09 Warnings Exact identifier application number: M020 Sunscreen and insect repellent Bull frog SPF 50 Bullfrog Brands, LLC d5fb3632-24da-2c7a-e053-2a95a90a5081 2025-01-09 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