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GUNA-DIUR

Generic: amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland -

Verified·Apr 23, 2026
Manufacturer
Guna
NDC
17089-260
Route
ORAL
ICD-10 indication
R60.9

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About GUNA-DIUR

What is this medication?

GUNA-DIUR is a homeopathic medicinal product formulated to address issues related to water retention and edema. It is typically used as a supportive treatment to stimulate the body's natural drainage processes, helping to reduce the accumulation of fluids in various tissues. The medication is often prescribed for conditions involving localized or generalized swelling, inflammatory states that contribute to fluid buildup, and as a way to provide generalized support for the excretory functions of the urinary system.

The formula consists of a combination of low-dose homeopathic ingredients, such as Apis mellifica and Berberis vulgaris, which work synergistically to promote kidney function and metabolic balance. By targeting specific physiological pathways, it helps the body eliminate excess fluids and metabolic waste more efficiently without the aggressive electrolyte depletion sometimes associated with conventional diuretics. It is frequently utilized in integrative medicine protocols for patients seeking to manage chronic swelling or as part of a broader detoxification and drainage regimen.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for GUNA-DIUR. Official source: DailyMed (NLM) · Label effective Dec 21, 2018

Indications and usage
1. INDICATIONS AND USAGE 1.1 Temporary relief of fluid retention 1.2 Tissue swelling and related disconforts
Dosage and 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.
Warnings and precautions
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.
Drug interactions
7. DRUG INTERACTIONS 7.1. None Known
Adverse reactions
6. ADVERSE REACTIONS 6.1. None known (see CONTRAINDICATIONS for hypersensitivity information).
Use in pregnancy
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.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

Conditions we've indexed resources for

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.