warnings
WARNINGS Stop use and ask doctor if symptoms of cough, shortness of breath, or wheezing do not improve, worsen or persist more than 3 days
GAMMA -12
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
- GAMMA -12
- Generic name
- INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B -
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c3366fcd-7d7a-4cf8-995c-798b6d2c9ad1
- SPL ID
- ed853c61-ca74-4c3d-e053-2995a90aecb9
- Version
- 5
- Effective date
- 2022-11-15
- Source export date
- 2026-09-28
- 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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:49
| 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 | GAMMA -12 | openfda.brand_name | |
| generic name | INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B - | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-405-18 | openfda.package_ndc |
| ndc | product | 17089-405 | openfda.product_ndc |
| ndc11 | package | 17089040518 | derived:openfda.package_ndc |
| spl id | ed853c61-ca74-4c3d-e053-2995a90aecb9 | id | |
| spl set id | c3366fcd-7d7a-4cf8-995c-798b6d2c9ad1 | set_id | |
| unii | 21K6M2I7AG | openfda.unii | |
| unii | 02FXP10O2U | 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.