warnings
WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 5 days. If pregnant or breast-feeding ask a doctor professional before use. Keep this and all medicines out of reach of children. Contains ethyl alcohol 30%
GUNA-IL 10
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 10
- Generic name
- INTERLEUKIN-10
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d6faade4-6263-44d3-b278-12088eb56e46
- SPL ID
- 53e9f2bb-21fd-d6c8-e063-6294a90ae615
- Version
- 6
- Effective date
- 2026-06-10
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:39
| 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 10 | openfda.brand_name | |
| generic name | INTERLEUKIN-10 | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-388-18 | openfda.package_ndc |
| ndc | product | 17089-388 | openfda.product_ndc |
| ndc11 | package | 17089038818 | derived:openfda.package_ndc |
| spl id | 53e9f2bb-21fd-d6c8-e063-6294a90ae615 | id | |
| spl set id | d6faade4-6263-44d3-b278-12088eb56e46 | set_id | |
| unii | 9SC4O216V9 | 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.