GUNA-DIUR
GUNA-DIUR is an FDA drug label for the active ingredient AMILORIDE - APIS MELLIFERA - BERBERIS VULGARIS FRUIT - HIERACIUM PILOSELLA FLOWERING TOP - HYDROCHLOROTHIAZIDE - SOLIDAGO VIRGAUREA FLOWERING TOP - SPIRONOLACTONE - SUS SCROFA PITUITARY GLAND - manufactured by Guna spa administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20181221.
- 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
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 17089-260
- Application
- N/A
- Label effective
- 20181221
About this product
GUNA-DIUR is an FDA-registered drug product whose active ingredient is AMILORIDE - APIS MELLIFERA - BERBERIS VULGARIS FRUIT - HIERACIUM PILOSELLA FLOWERING TOP - HYDROCHLOROTHIAZIDE - SOLIDAGO VIRGAUREA FLOWERING TOP - SPIRONOLACTONE - SUS SCROFA PITUITARY GLAND -. It is labelled by Guna spa taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 17089-260, label effective 20181221. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing AMILORIDE - APIS MELLIFERA - BERBERIS VULGARIS FRUIT - HIERACIUM PILOSELLA FLOWERING TOP - HYDROCHLOROTHIAZIDE - SOLIDAGO VIRGAUREA FLOWERING TOP - SPIRONOLACTONE - SUS SCROFA PITUITARY GLAND - are most often described in connection with: usage temporary, relief fluid, retention tissue, related disconforts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
1. INDICATIONS AND USAGE 1.1 Temporary relief of fluid retention 1.2 Tissue swelling and related disconforts
Dosage & Administration
2. 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.
Contraindications
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.
Adverse Reactions
6. ADVERSE REACTIONS 6.1. None known (see CONTRAINDICATIONS for hypersensitivity information).
Frequently asked questions
What is GUNA-DIUR used for?
1. INDICATIONS AND USAGE 1.1 Temporary relief of fluid retention 1.2 Tissue swelling and related disconforts
Who makes GUNA-DIUR?
Guna spa is the labeler of record for GUNA-DIUR.
What form does GUNA-DIUR come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is GUNA-DIUR prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has GUNA-DIUR been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.