Mineral Sunscreen 20percent Zinc Oxide
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
- Mineral Sunscreen 20percent Zinc Oxide
- Generic name
- ZINC OXIDE
- Manufacturer
- Mantra Wellness Spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 338a11fb-24c6-8a0b-e063-6294a90a761e
- SPL ID
- 45ffaf74-d6d0-d069-e063-6294a90a0b66
- Version
- 2
- Effective date
- 2025-12-15
- Source export date
- 2026-10-30
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:21:27
| 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 | Mineral Sunscreen 20percent Zinc Oxide | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Mantra Wellness Spa | openfda.manufacturer_name | |
| ndc | package | 85377-205-15 | openfda.package_ndc |
| ndc | product | 85377-205 | openfda.product_ndc |
| ndc11 | package | 85377020515 | derived:openfda.package_ndc |
| spl id | 45ffaf74-d6d0-d069-e063-6294a90a0b66 | id | |
| spl set id | 338a11fb-24c6-8a0b-e063-6294a90a761e | set_id | |
| unii | SOI2LOH54Z | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.