warnings
WARNINGS Stop use and ask doctor if symptoms of discomfort with swallowing or run down feeling worsen or persist more than 5 days
GUNA-REACT
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-REACT
- Generic name
- ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC -
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c2b64907-1ae2-4686-b13c-847dbb84724e
- SPL ID
- 7e7d6ebc-5974-b9fc-e053-2991aa0a2ae5
- Version
- 2
- Effective date
- 2018-12-21
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:58
| 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-REACT | openfda.brand_name | |
| generic name | ANGELICA SINENSIS ROOT - ARNICA MONTANA - ASIAN GINSENG - ECHINACEA ANGUSTIFOLIA - FOMITOPSIS PINICOLA FRUITING BODY - INTERFERON GAMMA-1B - PAEONIA OFFICINALIS ROOT - PORK LIVER - REISHI - SILYBUM MARIANUM SEED - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - TURMERIC - | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-237-20 | openfda.package_ndc |
| ndc | product | 17089-237 | openfda.product_ndc |
| ndc11 | package | 17089023720 | derived:openfda.package_ndc |
| spl id | 7e7d6ebc-5974-b9fc-e053-2991aa0a2ae5 | id | |
| spl set id | c2b64907-1ae2-4686-b13c-847dbb84724e | set_id | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 8R564U2E1P | openfda.unii | |
| unii | 308LM01C72 | openfda.unii | |
| unii | CUQ3A77YXI | openfda.unii | |
| unii | 856YO1Z64F | openfda.unii | |
| unii | 30D02U2IRN | openfda.unii | |
| unii | U946SH95EE | openfda.unii | |
| unii | VB06AV5US8 | openfda.unii | |
| unii | B66F4574UG | openfda.unii | |
| unii | 21K6M2I7AG | openfda.unii | |
| unii | 6EC706HI7F | openfda.unii | |
| unii | TKD8LH0X2Z | 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.