United States · FDA National Drug Code directory

GUNA-DIUR

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 17089-260_7e7c2115-72fe-9ca5-e053-2a91aa0ae101
Product NDC: 17089-260
Form: SOLUTION/ DROPS
Composition / generic term: amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland -
Labeler: Guna spa
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20060523
Source listing expiry: 20261231

Source-listed ingredients

AMILORIDE — 4 [hp_X]/30mL
APIS MELLIFERA — 2 [hp_X]/30mL
BERBERIS VULGARIS FRUIT — .3 g/30mL
HYDROCHLOROTHIAZIDE — 4 [hp_X]/30mL
SUS SCROFA PITUITARY GLAND — 12 [hp_X]/30mL
HIERACIUM PILOSELLA FLOWERING TOP — .3 g/30mL
SOLIDAGO VIRGAUREA FLOWERING TOP — .3 g/30mL
SPIRONOLACTONE — 4 [hp_X]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE, DROPPER in 1 BOX (17089-260-18) / 30 mL in 1 BOTTLE, DROPPER · 17089-260-18

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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