warnings
Warnings: For external use only. Avoid contact with eyes. Rinse with water to remove. Do not use on damaged or broken skin.
SPF 50 Daily UV Defense Broad Spectrum 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
- SPF 50 Daily UV Defense Broad Spectrum Sunscreen
- Generic name
- OCTINOXATE, ZINC OXIDE
- Manufacturer
- Vi Medical Products, INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2d814f8a-23b5-209f-e063-6394a90a5091
- SPL ID
- 37f244fd-c02e-e66a-e063-6394a90aed81
- Version
- 3
- Effective date
- 2025-06-19
- Source export date
- 2026-10-27
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:59:56
| 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 | SPF 50 Daily UV Defense Broad Spectrum Sunscreen | openfda.brand_name | |
| generic name | OCTINOXATE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Vi Medical Products, INC | openfda.manufacturer_name | |
| ndc | package | 70484-008-05 | openfda.package_ndc |
| ndc | package | 70484-008-06 | openfda.package_ndc |
| ndc | package | 70484-008-03 | openfda.package_ndc |
| ndc | package | 70484-008-01 | openfda.package_ndc |
| ndc | package | 70484-008-02 | openfda.package_ndc |
| ndc | package | 70484-008-04 | openfda.package_ndc |
| ndc | product | 70484-008 | openfda.product_ndc |
| ndc11 | package | 70484000802 | derived:openfda.package_ndc |
| ndc11 | package | 70484000803 | derived:openfda.package_ndc |
| ndc11 | package | 70484000805 | derived:openfda.package_ndc |
| ndc11 | package | 70484000801 | derived:openfda.package_ndc |
| ndc11 | package | 70484000804 | derived:openfda.package_ndc |
| ndc11 | package | 70484000806 | derived:openfda.package_ndc |
| spl id | 37f244fd-c02e-e66a-e063-6394a90aed81 | id | |
| spl set id | 2d814f8a-23b5-209f-e063-6394a90a5091 | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| unii | 4Y5P7MUD51 | 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.