Non-Tinted Mineral Foaming 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
- Non-Tinted Mineral Foaming Sunscreen
- Generic name
- TITANIUM DIOXIDE, ZINC OXIDE
- Manufacturer
- Restore Skin Therapy, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 364b6af2-a0ed-4a17-e063-6394a90a3a17
- SPL ID
- 459bfcc2-12be-82a9-e063-6294a90a6ca3
- Version
- 2
- Effective date
- 2025-12-10
- Source export date
- 2026-08-17
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-08-17/f57e66e711c6087f1ed24eae0e3950b4ffe20bc9d2d79cdb57444435ae535541/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
- Import run
- 20260818T065550Z
- Imported at
- 2026-08-18 07:09:17
| 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 | Non-Tinted Mineral Foaming Sunscreen | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Restore Skin Therapy, LLC | openfda.manufacturer_name | |
| ndc | package | 85313-211-04 | openfda.package_ndc |
| ndc | product | 85313-211 | openfda.product_ndc |
| ndc11 | package | 85313021104 | derived:openfda.package_ndc |
| spl id | 459bfcc2-12be-82a9-e063-6294a90a6ca3 | id | |
| spl set id | 364b6af2-a0ed-4a17-e063-6394a90a3a17 | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| unii | 15FIX9V2JP | openfda.unii |