GUNA-DIUR- amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - soli

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

AMILORIDE (UNII: 7DZO8EB0Z3) (AMILORIDE - UNII:7DZO8EB0Z3), APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z), BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3) (BERBERIS VULGARIS FRUIT - UNII:6XEF22AHC3), HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (HYDROCHLOROTHIAZIDE - UNII:0J48LPH2TH), SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND - UNII:E8S87O660T), HIERACIUM PILOSELLA FLOWERING TOP (UNII: 08A7Y81S1P) (HIERACIUM PILOSELLA FLOWERING TOP - UNII:08A7Y81S1P), SOLIDA

Available from:

Guna spa

Administration route:

ORAL

Prescription type:

PRESCRIPTION DRUG

Therapeutic indications:

1.1 Temporary relief of fluid retention 1.2 Tissue swelling and related disconforts 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. 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. 9.1.    No Known.

Product summary:

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).

Authorization status:

unapproved homeopathic

Summary of Product characteristics

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
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug Administration for_
_safety or efficacy. FDA is not aware of scientific evidence to
support homeopathy as effective._
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GUNA®-DIUR
1. INDICATIONS AND USAGE
1.1 Temporary relief of fluid retention
1.2 Tissue swelling and related disconforts
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.
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
6.1. None known (see CONTRAINDICATIONS for hypersensitivity
information).
7. DRUG INTERACTIONS
7.1. None Known
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 wheth