Ultra Zinc Mineral Non Tinted
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
- Ultra Zinc Mineral Non Tinted
- Generic name
- ZINC OXIDE
- Manufacturer
- Skin Therapy Studio LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3545d603-3d01-c51d-e063-6394a90a1599
- SPL ID
- 46002ad3-8c61-8593-e063-6394a90a6b67
- Version
- 2
- Effective date
- 2025-12-15
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:47:24
| 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 | Ultra Zinc Mineral Non Tinted | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Skin Therapy Studio LLC | openfda.manufacturer_name | |
| ndc | package | 85357-205-04 | openfda.package_ndc |
| ndc | product | 85357-205 | openfda.product_ndc |
| ndc11 | package | 85357020504 | derived:openfda.package_ndc |
| spl id | 46002ad3-8c61-8593-e063-6394a90a6b67 | id | |
| spl set id | 3545d603-3d01-c51d-e063-6394a90a1599 | set_id | |
| unii | SOI2LOH54Z | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.