warnings
Stop using it immediately if there are signs of skin rashes or hypersensitivity.
Vita Soluball
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
- Vita Soluball
- Generic name
- ASCORBIC ACID, ZINC OXIDE
- Manufacturer
- Silexn Technology Co.,Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0fa7105d-ee23-d73a-e063-6394a90a34f0
- SPL ID
- 0fa71049-16a4-c0db-e063-6294a90a7edf
- Version
- 1
- Effective date
- 2024-01-23
- Source export date
- 2026-10-27
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:58:52
| 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 |
|---|---|---|---|
| brand name | Vita Soluball | openfda.brand_name | |
| generic name | ASCORBIC ACID, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Silexn Technology Co.,Ltd. | openfda.manufacturer_name | |
| ndc | package | 84020-0001-1 | openfda.package_ndc |
| ndc | product | 84020-0001 | openfda.product_ndc |
| ndc11 | package | 84020000101 | derived:openfda.package_ndc |
| spl id | 0fa71049-16a4-c0db-e063-6294a90a7edf | id | |
| spl set id | 0fa7105d-ee23-d73a-e063-6394a90a34f0 | set_id | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | SOI2LOH54Z | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.