Non Tinted Moisturizing 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
- Non Tinted Moisturizing Mineral Sunscreen
- Generic name
- ZINC OXIDE
- Manufacturer
- EDIT EUROSPA, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3751e278-b8b2-7bf4-e063-6394a90a4290
- SPL ID
- 4604a39a-68bf-7dd9-e063-6394a90a5515
- Version
- 2
- Effective date
- 2025-12-15
- Source export date
- 2026-10-30
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:26:39
| 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 Moisturizing Mineral Sunscreen | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | EDIT EUROSPA, LLC | openfda.manufacturer_name | |
| ndc | package | 85642-205-04 | openfda.package_ndc |
| ndc | product | 85642-205 | openfda.product_ndc |
| ndc11 | package | 85642020504 | derived:openfda.package_ndc |
| spl id | 4604a39a-68bf-7dd9-e063-6394a90a5515 | id | |
| spl set id | 3751e278-b8b2-7bf4-e063-6394a90a4290 | set_id | |
| unii | SOI2LOH54Z | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.