Parasol Daily Mineral 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
- Parasol Daily Mineral Sunscreen
- Generic name
- ZINC OXIDE
- Manufacturer
- Bodi & Wax, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 35d3262a-1d8d-2afa-e063-6294a90afd49
- SPL ID
- 4604493b-6ab7-843d-e063-6294a90a574d
- Version
- 2
- Effective date
- 2025-12-15
- Source export date
- 2026-10-12
- 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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:33:11
| 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 | Parasol Daily Mineral Sunscreen | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Bodi & Wax, LLC | openfda.manufacturer_name | |
| ndc | package | 85373-208-15 | openfda.package_ndc |
| ndc | product | 85373-208 | openfda.product_ndc |
| ndc11 | package | 85373020815 | derived:openfda.package_ndc |
| spl id | 4604493b-6ab7-843d-e063-6294a90a574d | id | |
| spl set id | 35d3262a-1d8d-2afa-e063-6294a90afd49 | set_id | |
| unii | SOI2LOH54Z | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.