GUNA-DIUR
- Product NDC
- 17089-260
- 11-digit product format
- 170890260
- Labeler code
- 17089
- Product ID
- 17089-260_7e7c2115-72fe-9ca5-e053-2a91aa0ae101
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland -
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Labeler
- Guna spa
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2006-05-23
- Substance
- AMILORIDE; APIS MELLIFERA; BERBERIS VULGARIS FRUIT; HIERACIUM PILOSELLA FLOWERING TOP; HYDROCHLOROTHIAZIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; SPIRONOLACTONE; SUS SCROFA PITUITARY GLAND
- Active strength
- 4; 2; .3; .3; 4; .3; 4; 12 [hp_X]/30mL; [hp_X]/30mL; g/30mL; g/30mL; [hp_X]/30mL; g/30mL; [hp_X]/30mL; [hp_X]/30mL
- Pharmacologic classes
- Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Potassium-sparing Diuretic [EPC], Standardized Insect Venom Allergenic Extract [EPC], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GUNA-DIUR
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| AMILORIDE | 4 [hp_X]/30mL |
| APIS MELLIFERA | 2 [hp_X]/30mL |
| BERBERIS VULGARIS FRUIT | .3 g/30mL |
| HIERACIUM PILOSELLA FLOWERING TOP | .3 g/30mL |
| HYDROCHLOROTHIAZIDE | 4 [hp_X]/30mL |
| SOLIDAGO VIRGAUREA FLOWERING TOP | .3 g/30mL |
| SPIRONOLACTONE | 4 [hp_X]/30mL |
| SUS SCROFA PITUITARY GLAND | 12 [hp_X]/30mL |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | 7DZO8EB0Z3, 7S82P3R43Z, 6XEF22AHC3, 08A7Y81S1P, 0J48LPH2TH, 5405K23S50, 27O7W4T232, L0PFEMQ1DT |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17089-260-18 | GUNA-DIUR | 1 in 1 BOX | SOLUTION/ DROPS | 1 | 2 | |
| 17089-260-18 | GUNA-DIUR | 30 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 30 | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17089-260 | GUNA-DIUR (AMILORIDE - APIS MELLIFERA - BERBERIS VULGARIS FRUIT - HIERACIUM PILOSELLA FLOWERING TOP - HYDROCHLOROTHIAZIDE - SOLIDAGO VIRGAUREA FLOWERING TOP - SPIRONOLACTONE - SUS SCROFA PITUITARY GLAND -) SOLUTION/ DROPS [GUNA SPA] | 2 | Current NDC, Legacy NDC, 2 package rows | 20190405_3f91cd92-eb6d-4bda-9cad-2e11e0b0fbe2.zip |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 17089-260-18 | 17089026018 | 1 BOTTLE, DROPPER in 1 BOX (17089-260-18) / 30 mL in 1 BOTTLE, DROPPER | 2018-12-21 | 0000-00-00 | No | No | Current |