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GUNA-DIUR

Active substance: AMILORIDE, APIS MELLIFERA, BERBERIS VULGARIS FRUIT, HYDROCHLOROTHIAZIDE, SUS SCROFA PITUITARY GLAND, HIERACIUM PILOSELLA FLOWERING TOP, SOLIDAGO VIRGAUREA FLOWERING TOP, SPIRONOLACTONE

SOLUTION/ DROPS · 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

United StatesActive

Marketing holder: Guna spa

Verified 2026-10-09 · openFDA NDC

Composition
  • 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
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-6594-7a8b-8277-3cae6671924a,01a12093-69cb-741a-b737-d93887a2b6b8,01a1209c-271c-7403-abf5-60cacfc45dd5;count=3 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
17089-260
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 17089-260 · Verified 2026-10-09 · open in source