GUNA®-DIURGuna spaGuna spaGUNA-DIURamiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland -ALCOHOLAMILORIDEAMILORIDEAPIS MELLIFERAAPIS MELLIFERABERBERIS VULGARIS FRUITBERBERIS VULGARIS FRUITHYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDESUS SCROFA PITUITARY GLANDSUS SCROFA PITUITARY GLANDHIERACIUM PILOSELLA FLOWERING TOPHIERACIUM PILOSELLA FLOWERING TOPSOLIDAGO VIRGAUREA FLOWERING TOPSOLIDAGO VIRGAUREA FLOWERING TOPSPIRONOLACTONESPIRONOLACTONE1. INDICATIONS AND USAGE
1.1 Temporary relief of fluid retention
1.2 Tissue swelling and related disconforts
2. DOSAGE AND ADMINISTRATIONAdults: 20 drops in a little water, 2 times per day for an avarage of two months.Stop use and ask a doctor if symptoms persist more than 5 days.Administration may very according to individual needs.GUNA-DIUR may be used together with other homeopthic medicines.3. DOSAGE FORMS AND STRENGTHS3.1. 30 ml Bottle dropper container contains:
Active ingredients: Amiloride 4X 0.006 ml, Apis Mellifica 2X 0.626 ml, Berberis Vulgaris T 0.314 ml, Hydrochlorothiazide 4X 0.006 ml, Hypophysis 12X 6.314 ml, Mouse-Ear Hawkweed T 6.314 ml, Solidago Virgaurea T 0.314 ml, Spironolactone 4X 0.006 ml.
Inactive Ingredient: Ethylic Alcohol 30%
4. CONTRAINDICATIONS4.1. There is no history of hypersensitivity to GUNA-DIUR. However, do not use if you are hypersensitive to any of the active ingredients of Guna-Diur.5. WARNINGS AND PRECAUTIONS5.1. 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.
6. ADVERSE REACTIONS6.1. None known (see CONTRAINDICATIONS for hypersensitivity information).
7. DRUG INTERACTIONS7.1. None Known
8. USE IN SPECIFIC POPULATIONS8.1.
Pregnancy: Pregnancy category C. Animal reproduction studies have not been conducted with GUNA-DIUR. GUNA®- DIUR should not be given to a pregnant woman.
8.2.
Lactation: It is not known whether any of the ingredients in GUNA- DIUR are secreted in human milk. However, since many drugs are secreted in human milk, caution should be exercised when GUNA- DIUR is administered to a nursing woman.
8.3.
Pediatric use: Safety and effectiveness in pediatric patients have not been established.
8.4.
Geriatric use: No restrictions.
9. DRUG ABUSE AND DEPENDENCE9.1. No Known.10. OVERDOSAGE10.1. No Known.
11. DESCRIPTION11. 1 GUNA-DIUR is a homeopathic medicine indicated for the temporary relief of fluid retention, tissue swelling and related disconforts.12. CLINICAL PHARMACOLOGY12.1. GUNA-DIUR exerts a diuretic effect. This is based on homeopthica Materia Medica and homeopathic principles.
12.2. Pharmacodynamics
Not applicable to homeopthic medicinal products.
12.3. PharmacokineticsNot applicable to homeopthic medicinal products. 13. NONCLINICAL TOXICOLOGY13.1. Not available.
14. CLINICAL STUDIES14.1. GUNA-DIUR efficacy is not supported by clinical studies. It is based on homeopathic Materia Medica and scientific literature.
15. REFERENCES15.1. H.H. Reckeweg. Homeopathic Materia Medica. Aurelia Verlag.
15.2. Boericke, William, Materia Medica with Reperatory, 1927, ninth edition
16. HOW SUPPLIED/STORAGE AND HANDLING16.1. NDC 17089-260-18 Oral Solution/Drops 30 mL
16.2. Store at 20-25°C (68-77° F). Excursions permitted between 15°-30°C (59°-86°F).
17. PATIENT COUNSELING INFORMATION17.1. Patients should be informed about Homeopathy and the main differences with conventional clinical approaches.
PACKAGE LABEL5USPIL-GUNA-DIUR-rev05-10-18