GUNA-DIUR
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-DIUR
- Generic name
- AMILORIDE - APIS MELLIFERA - BERBERIS VULGARIS FRUIT - HIERACIUM PILOSELLA FLOWERING TOP - HYDROCHLOROTHIAZIDE - SOLIDAGO VIRGAUREA FLOWERING TOP - SPIRONOLACTONE - SUS SCROFA PITUITARY GLAND -
- Manufacturer
- Guna spa
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 3f91cd92-eb6d-4bda-9cad-2e11e0b0fbe2
- SPL ID
- 7e7c2115-72fe-9ca5-e053-2a91aa0ae101
- 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 05:55:51
| 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-DIUR | openfda.brand_name | |
| generic name | AMILORIDE - APIS MELLIFERA - BERBERIS VULGARIS FRUIT - HIERACIUM PILOSELLA FLOWERING TOP - HYDROCHLOROTHIAZIDE - SOLIDAGO VIRGAUREA FLOWERING TOP - SPIRONOLACTONE - SUS SCROFA PITUITARY GLAND - | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-260-18 | openfda.package_ndc |
| ndc | product | 17089-260 | openfda.product_ndc |
| ndc11 | package | 17089026018 | derived:openfda.package_ndc |
| spl id | 7e7c2115-72fe-9ca5-e053-2a91aa0ae101 | id | |
| spl set id | 3f91cd92-eb6d-4bda-9cad-2e11e0b0fbe2 | set_id | |
| unii | 7DZO8EB0Z3 | openfda.unii | |
| unii | 08A7Y81S1P | openfda.unii | |
| unii | 6XEF22AHC3 | openfda.unii | |
| unii | L0PFEMQ1DT | openfda.unii | |
| unii | 0J48LPH2TH | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | 27O7W4T232 | openfda.unii | |
| unii | 5405K23S50 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5. WARNINGS AND PRECAUTIONS 5.1. GUNA-DIUR is contraindicated in patients with anuria and in patients with a history of hypersensitivity to Spironolactone, Amiloride, or Hydrocholorthiazide. 5.2. Use with caution in patients taking diuretic medications. 5.3 Keep out of reach of children.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6. ADVERSE REACTIONS 6.1. None known (see CONTRAINDICATIONS for hypersensitivity information).
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.