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 144 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Non-Tinted Foaming Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE AESTHETICS ACADEMY, LLC 3698c076-68b1-7d28-e063-6394a90a517c 2025-12-09 Exact identifier application number: M020 Non-Tinted Replenishing Daily Protection ZINC OXIDE THE AESTHETICS ACADEMY, LLC 3699159a-3561-9ff6-e063-6394a90af9fd 2025-12-09 Exact identifier application number: M020 Sheer Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Rhonda J Pomerantz MD PLLC 325c1723-fb1d-ae3c-e063-6294a90a4609 2025-12-09 Exact identifier application number: M020 Sheer Mineral Sunscreen Satin Dewy Finish ZINC OXIDE TRU SKIN RITUALS 3249d05b-0f5c-4787-e063-6294a90aa0d7 2025-12-09 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Rhonda J Pomerantz MD PLLC 325c3a18-ba8f-912d-e063-6394a90a2447 2025-12-09 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Rhonda J Pomerantz MD PLLC 325c8641-1161-b8ac-e063-6394a90ae451 2025-12-09 Exact identifier application number: M020 Sheer Mineral Sunscreen Silk Matte Finish TITANIUM DIOXIDE, ZINC OXIDE TRU SKIN RITUALS 3248eb22-1e10-2091-e063-6394a90ad3e1 2025-12-09 Exact identifier application number: M020 Tinted Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Rhonda J Pomerantz MD PLLC 325cce54-a885-d586-e063-6394a90a90db 2025-12-09 Exact identifier application number: M020 Sheer Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE TRU SKIN RITUALS 324acd75-9c38-4adc-e063-6394a90afa12 2025-12-09 Exact identifier application number: M020 Sheer Mineral Sunscreen Satin Dewy Finish ZINC OXIDE TRU SKIN RITUALS 324960e6-c1e7-d2b9-e063-6294a90a92ce 2025-12-09 Exact identifier application number: M020 Sol Purpose Mineral Sunscreen Tinted ZINC OXIDE TRU SKIN RITUALS 324a3475-07f0-033c-e063-6394a90a811a 2025-12-09 Exact identifier application number: M020 Perfect Sunscreen SPF 50 Sheer Mineral ZINC OXIDE Bluemercury, Inc. d8f483ff-b990-40c5-b5b8-00065051ae7e 2025-12-09 Warnings Exact identifier application number: M020 Foto Facial Age Delay Non-Tinted TITANIUM DIOXIDE ZINC OXIDE ADVANCED AESTHETIC DERMATOLOGY 42674013-fa2b-42d7-e063-6294a90af999 2025-12-09 Warnings Exact identifier application number: M020 Hydraboost Moisturizer SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE Bluemercury eca867e6-4deb-4be2-ae3f-6850fb6223b3 2025-12-09 Warnings Exact identifier application number: M020 Foto Facial Age Delay Matte Tinted TITANIUM DIOXIDE ZINC OXIDE ADVANCED AESTHETIC DERMATOLOGY 42761919-8ae2-3c41-e063-6394a90abb8f 2025-12-09 Warnings Exact identifier application number: M020 Dew Mineral ZINC OXIDE ADVANCED AESTHETIC DERMATOLOGY 42f17245-92a9-3915-e063-6394a90a6817 2025-12-09 Warnings Exact identifier application number: M020 Mineral Sunscreen Non-Tinted TITANIUM DIOXIDE, ZINC OXIDE YUMA ACNE CLINIC, L.L.C. 3c69b707-07ff-1a82-e063-6394a90a9fcd 2025-12-09 Warnings Exact identifier application number: M020 Mineral Sunscreen Tinted TITANIUM DIOXIDE, ZINC OXIDE YUMA ACNE CLINIC, L.L.C. 3c69f93f-0385-365c-e063-6394a90a12fd 2025-12-09 Warnings Exact identifier application number: M020 Replenishing Daily Protection Tinted ZINC OXIDE YUMA ACNE CLINIC, L.L.C. 3c6a5601-a7a2-5e20-e063-6394a90a6643 2025-12-09 Warnings Exact identifier application number: M020 Bronzing Blendrops Broad Spectrum SPF 40 HOMOSALATE, OCTISALATE, ZINC OXIDE Wasatch Product Development, LLC 124ca946-8412-4d6d-e063-6294a90a6338 2025-12-09 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