warnings
Warnings For external use only
La Roche Posay New 50 Body and Face SPF 50 Mineral Anthelios Gentle 100 percent mineral UV filters Soft finish with Cell Ox Shield
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 New 50 Body and Face SPF 50 Mineral Anthelios Gentle 100 percent mineral UV filters Soft finish with Cell Ox Shield
- Generic name
- TITANIUM DIOXIDE AND ZINC OXIDE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c0f7ae46-7161-4d48-9386-007bfafecfd5
- SPL ID
- 5e3f83d1-03e6-4aff-b18c-5286ee1da034
- Version
- 15
- Effective date
- 2024-01-01
- 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 New 50 Body and Face SPF 50 Mineral Anthelios Gentle 100 percent mineral UV filters Soft finish with Cell Ox Shield | 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 | 49967-091-01 | openfda.package_ndc |
| ndc | package | 49967-091-03 | openfda.package_ndc |
| ndc | package | 49967-091-05 | openfda.package_ndc |
| ndc | package | 49967-091-04 | openfda.package_ndc |
| ndc | package | 49967-091-02 | openfda.package_ndc |
| ndc | product | 49967-091 | openfda.product_ndc |
| ndc11 | package | 49967009104 | derived:openfda.package_ndc |
| ndc11 | package | 49967009101 | derived:openfda.package_ndc |
| ndc11 | package | 49967009105 | derived:openfda.package_ndc |
| ndc11 | package | 49967009102 | derived:openfda.package_ndc |
| ndc11 | package | 49967009103 | derived:openfda.package_ndc |
| spl id | 5e3f83d1-03e6-4aff-b18c-5286ee1da034 | id | |
| spl set id | c0f7ae46-7161-4d48-9386-007bfafecfd5 | 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.