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-TONSILS
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-TONSILS
- Generic name
- ANGELICA SINENSIS ROOT - BINETRAKIN - INTERLEUKIN-3 - LENOGRASTIM - MELATONIN - REISHI - SHIITAKE MUSHROOM - SUS SCROFA BLOOD - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - SUS SCROFA SPLEEN - INTERLEUKIN-11 -
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b7d0a24f-c702-4b4a-8494-a4cbbb020257
- SPL ID
- 7e8f9d55-ff7c-cbe7-e053-2a91aa0a382e
- Version
- 4
- Effective date
- 2018-12-21
- Source export date
- 2026-09-28
- 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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:45
| 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-TONSILS | openfda.brand_name | |
| generic name | ANGELICA SINENSIS ROOT - BINETRAKIN - INTERLEUKIN-3 - LENOGRASTIM - MELATONIN - REISHI - SHIITAKE MUSHROOM - SUS SCROFA BLOOD - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - SUS SCROFA SPLEEN - INTERLEUKIN-11 - | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-235-20 | openfda.package_ndc |
| ndc | product | 17089-235 | openfda.product_ndc |
| ndc11 | package | 17089023520 | derived:openfda.package_ndc |
| spl id | 7e8f9d55-ff7c-cbe7-e053-2a91aa0a382e | id | |
| spl set id | b7d0a24f-c702-4b4a-8494-a4cbbb020257 | set_id | |
| unii | 308LM01C72 | openfda.unii | |
| unii | VPB6TR49WU | openfda.unii | |
| unii | 92AMN5J79Y | openfda.unii | |
| unii | 751635Z921 | openfda.unii | |
| unii | B66F4574UG | openfda.unii | |
| unii | 6WS4C399GB | openfda.unii | |
| unii | O14Q7A13PT | openfda.unii | |
| unii | JL5DK93RCL | openfda.unii | |
| unii | TKD8LH0X2Z | openfda.unii | |
| unii | 1A64QN2D2F | 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.