Guna-Diur: Package Insert / Prescribing Info
Package insert / product label
Generic name: amiloride, apis mellifera, berberis vulgaris fruit, hydrochlorothiazide, sus scrofa pituitary gland, hieracium pilosella flowering top, solidago virgaurea flowering top and spironolactone
Dosage form: oral solution / drops
On This Page
- Indications and Usage
- Dosage and Administration
- Dosage Forms and Strengths
- Contraindications
- Warnings and Precautions
- Adverse Reactions/Side Effects
- Drug Interactions
- Use In Specific Populations
- Drug Abuse and Dependence
- Overdosage
- Description
- Clinical Pharmacology
- Nonclinical Toxicology
- Clinical Studies
- References
- Storage and Handling
- Patient Counseling Information
1. Indications and Usage for Guna-Diur
1.1 Temporary relief of fluid retention
1.2 Tissue swelling and related disconforts
2. Guna-Diur Dosage and Administration
Adults: 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 Strengths
3.1. 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. Contraindications
4.1. 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 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.
6. Adverse Reactions/Side Effects
6.1. None known (see CONTRAINDICATIONS for hypersensitivity information).
8. Use In Specific Populations
8.1.
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.
11. Guna-Diur Description
11. 1 GUNA-DIUR is a homeopathic medicine indicated for the temporary relief of fluid retention, tissue swelling and related disconforts.
12. Guna-Diur - Clinical Pharmacology
12.1. 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. Pharmacokinetics
Not applicable to homeopthic medicinal products.
14. Clinical Studies
14.1. GUNA-DIUR efficacy is not supported by clinical studies. It is based on homeopathic Materia Medica and scientific literature.
15. References
15.1. H.H. Reckeweg. Homeopathic Materia Medica. Aurelia Verlag.
15.2. Boericke, William, Materia Medica with Reperatory, 1927, ninth edition
16. Storage and Handling
16.1. 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).
GUNA-DIUR
amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland - solution/ drops |
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Labeler - Guna spa (430538264) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Guna spa | 338587646 | manufacture(17089-260) |