warnings
WARNINGS Stop use and ask doctor if symptoms persist more than 5 days or worsen. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children.
GUNA-VIRUS
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-VIRUS
- Generic name
- ALDESLEUKIN - EVERLASTING EXTRACT - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - MELATONIN - METENKEFALIN - REISHI - SEROTONIN - SOYBEAN - SUS SCROFA BLOOD - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - SUS SCROFA SPLEEN -
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 53e741c4-8897-71f3-e063-6394a90a751d
- SPL ID
- 53e75d71-d919-2bc0-e063-6294a90a1d7f
- Version
- 1
- Effective date
- 2026-07-01
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:32
| 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-VIRUS | openfda.brand_name | |
| generic name | ALDESLEUKIN - EVERLASTING EXTRACT - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - MELATONIN - METENKEFALIN - REISHI - SEROTONIN - SOYBEAN - SUS SCROFA BLOOD - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - SUS SCROFA SPLEEN - | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-503-20 | openfda.package_ndc |
| ndc | product | 17089-503 | openfda.product_ndc |
| ndc11 | package | 17089050320 | derived:openfda.package_ndc |
| spl id | 53e75d71-d919-2bc0-e063-6294a90a1d7f | id | |
| spl set id | 53e741c4-8897-71f3-e063-6394a90a751d | set_id | |
| unii | 308LM01C72 | openfda.unii | |
| unii | KQV867ADR4 | openfda.unii | |
| unii | 30D02U2IRN | openfda.unii | |
| unii | 9JEZ9OD3AS | openfda.unii | |
| unii | 92AMN5J79Y | openfda.unii | |
| unii | 333DO1RDJY | openfda.unii | |
| unii | M89N0Q7EQR | openfda.unii | |
| unii | L7HT8F1ZOD | openfda.unii | |
| unii | 21K6M2I7AG | openfda.unii | |
| unii | JL5DK93RCL | openfda.unii | |
| unii | TKD8LH0X2Z | openfda.unii | |
| unii | 994R458ECK | 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.