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
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 49967-907 | 49967-907-02 | D | Discontinued by firm | 2026-10-16 |
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.
| 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 |
|---|---|
| TITANIUM DIOXIDE | 60 mg/mL |
| ZINC OXIDE | 50 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 15FIX9V2JP | Internal UNII lookup |
| SOI2LOH54Z | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2ce83dc2-84b6-43fd-8b11-495d41cebc22 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c6f86816-7da6-43ea-8c25-ac9758311cc5 | Product name | 1 | 20220118 |
| 252e11b6-1a9a-4283-a242-df2c129c496d | Product name | 3 | 20170717 |
DailyMed Package Descriptions#
| 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#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Titanium dioxide | ACTIVE INGREDIENT | 15FIX9V2JP | LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC] | 7 | |
| Zinc oxide | ACTIVE INGREDIENT | SOI2LOH54Z | LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC] | 7 | |
| Titanium dioxide | ACTIVE MOIETY | 15FIX9V2JP | LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC] | 7 | |
| Zinc oxide | ACTIVE MOIETY | SOI2LOH54Z | LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC] | 7 |
DailyMed Dashboard NDC Coverage#
| 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Jack Black | AVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUM | Jack Black L.L.C. | 4bad1502-bc44-54ec-e063-6294a90ace8b | 2026-02-25 | Warnings | M020 |
| Truskin SPF 30 Mineral Sunscreen Facial Serum | ZINC OXIDE | Allure Labs | 2e20c132-8a03-1d5d-e063-6394a90ad2c3 | 2026-02-25 | Warnings | M020 |
| Rationale The Brilliance Tinted Serum SPF 50 | ZINC OXIDE | RATIONALE GROUP PTY LTD | 5c38506b-1533-435f-87a6-0452bae5b29f | 2026-02-24 | Warnings | M020 |
| FULLY RICE CERAMIDE MOISTURE SUNSCREEN | ZINC OXIDE | Adapt Inc. | d8bfe222-3184-4c98-9876-ef5ac81772b6 | 2026-02-24 | Warnings | M020 |
| cle de peau BEAUTE THE FOUNDATION N M O20 | OCTINOXATE AND TITANIUM DIOXIDE | Shiseido Americas Corporation | 9507f6d1-c11c-428d-8d95-b436f27ba26a | 2026-02-24 | Warnings | M020 |
| Perfect Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | SKIN PERFECT MEDICAL | 4b93538a-3b3e-90f7-e063-6294a90ab898 | 2026-02-24 | Warnings | M020 |
| ANTI-AGING TINTED SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | LASER GIRL SKINCARE, LLC | 4b93cd22-1289-29bc-e063-6294a90ab781 | 2026-02-24 | Warnings | M020 |
| ANTI-AGING TINTED SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | LASER GIRL SKINCARE, LLC | 4b943d72-dcde-e2e4-e063-6294a90ab7c4 | 2026-02-24 | Warnings | M020 |
| ANTI-AGING NON-TINTED SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | LASER GIRL SKINCARE, LLC | 4b946c39-718b-d70e-e063-6394a90a0db8 | 2026-02-24 | Warnings | M020 |
| Reunited Lipgloss SPF 30 - BTCH IS BACK | HOMOSALATE, OCTOCRYLENE, OCTISALATE | Princeville Productions, LLC, DBA Reunited Beauty | 4b961531-fbca-d1cf-e063-6294a90ab9a1 | 2026-02-24 | Warnings | M020 |
| sunscreen | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Meijer, Inc. | 8f5e634c-765b-4ffe-bb12-753d64c90cf9 | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | e97bf30a-1465-4912-bd55-1e7dd993132b | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | 67efcd94-00af-477b-bd14-d1c7b95d305a | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | 3f3d2e1e-1e95-4719-8ca9-83b6b804ab9f | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Sheer Touch Sunscreen Mist SPF 100 | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | f642788c-3643-459a-b736-0c06d0cd32a9 | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | 95ba2b33-f593-4e95-bd6e-5910d6aa5158 | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | 3b85004a-8832-4eac-bd70-1e607ae7af4b | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | 7f0fc23b-2d70-4426-9d64-a6d2b643309f | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Sport Sunscreen SPF 70 | AVOBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | 0ae9edd8-bf76-4bb2-ab78-c43c017ba4a5 | 2026-02-24 | Warnings, Adverse reactions | M020 |
| Avbenzone, Homosalate, Octisalate | AVBENZONE, HOMOSALATE, OCTISALATE | Meijer, Inc. | f8960995-66b6-4197-8976-b318fe01488f | 2026-02-24 | Warnings, Adverse reactions | M020 |
Packages#
| 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 |