warnings
Warnings For external use only
La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Broad Spectrum SPF 50 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 Broad Spectrum SPF 50 Sunscreen
- Generic name
- TITANIUM DIOXIDE AND ZINC OXIDE
- Manufacturer
- Cosmetique Active Production
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4e56f3f2-b856-4bbc-ab39-6fb5887a4846
- SPL ID
- 52bd923b-28c8-4baf-afca-eeac9d5adb70
- Version
- 2
- Effective date
- 2023-12-13
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:46
| 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 Broad Spectrum SPF 50 Sunscreen | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE AND ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Cosmetique Active Production | openfda.manufacturer_name | |
| ndc | package | 69625-908-02 | openfda.package_ndc |
| ndc | package | 69625-908-03 | openfda.package_ndc |
| ndc | package | 69625-908-01 | openfda.package_ndc |
| ndc | product | 69625-908 | openfda.product_ndc |
| ndc11 | package | 69625090802 | derived:openfda.package_ndc |
| ndc11 | package | 69625090803 | derived:openfda.package_ndc |
| ndc11 | package | 69625090801 | derived:openfda.package_ndc |
| spl id | 52bd923b-28c8-4baf-afca-eeac9d5adb70 | id | |
| spl set id | 4e56f3f2-b856-4bbc-ab39-6fb5887a4846 | 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.