warnings
Warnings For external use only . Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. If swallowed, get medical help, or contact a Poison Control Center right away.
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
| Harmonized routes |
|---|
| TOPICAL |
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 | SEYTU Facial Sunscreen | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE AND ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Omnilife USA, Inc. | openfda.manufacturer_name | |
| ndc | package | 84271-000-00 | openfda.package_ndc |
| ndc | product | 84271-000 | openfda.product_ndc |
| ndc11 | package | 84271000000 | derived:openfda.package_ndc |
| spl id | 3d2ac1ee-ae05-4012-84e1-58ed9d287e83 | id | |
| spl set id | 96fd37fb-c3ff-413f-b2c8-50754f320ecc | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| unii | 15FIX9V2JP | openfda.unii |
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse event summaries are temporarily unavailable. Other product information remains available.