warnings
Warnings For external use only
La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen
- Generic name
- TITANIUM DIOXIDE AND ZINC OXIDE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2ce83dc2-84b6-43fd-8b11-495d41cebc22
- SPL ID
- 93f2cacd-67af-4ad8-9e0a-4de8330f808f
- Version
- 17
- Effective date
- 2023-12-13
- Source export date
- 2026-11-06
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/f699a9578a0c5d6f5abd59491e85ce3c2c5e4567a51003fee350566c56ba5812/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:25:49
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M020 | openfda.application_number | |
| brand name | La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE AND ZINC OXIDE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-907-03 | openfda.package_ndc |
| ndc | package | 49967-907-02 | openfda.package_ndc |
| ndc | package | 49967-907-01 | openfda.package_ndc |
| ndc | product | 49967-907 | openfda.product_ndc |
| ndc11 | package | 49967090703 | derived:openfda.package_ndc |
| ndc11 | package | 49967090701 | derived:openfda.package_ndc |
| ndc11 | package | 49967090702 | derived:openfda.package_ndc |
| spl id | 93f2cacd-67af-4ad8-9e0a-4de8330f808f | id | |
| spl set id | 2ce83dc2-84b6-43fd-8b11-495d41cebc22 | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| unii | 15FIX9V2JP | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.