Ultimate Physical 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
- Ultimate Physical Sunscreen
- Generic name
- ZINC OXIDE
- Manufacturer
- HALEM DERMATOLOGY PLLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 35be5dc0-861f-3738-e063-6394a90a23ca
- SPL ID
- 45b3b915-94a5-405e-e063-6294a90a666e
- Version
- 2
- Effective date
- 2025-12-11
- Source export date
- 2026-10-30
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:08:24
| 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 | Ultimate Physical Sunscreen | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | HALEM DERMATOLOGY PLLC | openfda.manufacturer_name | |
| ndc | package | 85413-205-13 | openfda.package_ndc |
| ndc | product | 85413-205 | openfda.product_ndc |
| ndc11 | package | 85413020513 | derived:openfda.package_ndc |
| spl id | 45b3b915-94a5-405e-e063-6294a90a666e | id | |
| spl set id | 35be5dc0-861f-3738-e063-6394a90a23ca | set_id | |
| unii | SOI2LOH54Z | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.