warnings
WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 5 days
GUNA-IL 2
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
- GUNA-IL 2
- Generic name
- ALDESLEUKIN
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0619f291-207a-4e01-96bd-b882726665e2
- SPL ID
- ed8137f8-9931-234c-e053-2a95a90a5769
- Version
- 5
- Effective date
- 2022-11-15
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:33:38
| Harmonized routes |
|---|
| ORAL |
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 | GUNA-IL 2 | openfda.brand_name | |
| generic name | ALDESLEUKIN | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-380-18 | openfda.package_ndc |
| ndc | product | 17089-380 | openfda.product_ndc |
| ndc11 | package | 17089038018 | derived:openfda.package_ndc |
| spl id | ed8137f8-9931-234c-e053-2a95a90a5769 | id | |
| spl set id | 0619f291-207a-4e01-96bd-b882726665e2 | set_id | |
| unii | M89N0Q7EQR | 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.