17089-260 : Guna-diur Oral Solution/ Drops


NDC: 17089-260
Labeler: Guna Spa
Product Type: Human Prescription Drug
Drug Name: Guna-diur
Dosage Form: Oral Solution/ Drops
Rev. Date: 


NDC Package Codes:

  • 17089-260-18: 1 BOTTLE, DROPPER IN 1 BOX (17089‑260‑18) > 30 ML IN 1 BOTTLE, DROPPER

Active Ingredients:

  • Amiloride
  • Apis Mellifera
  • Berberis Vulgaris Fruit
  • Hydrochlorothiazide
  • Sus Scrofa Pituitary Gland
  • Hieracium Pilosella Flowering Top
  • Solidago Virgaurea Flowering Top
  • Spironolactone

Dosage Strength:

  • 4 [hp_X]/30mL
  • 2 [hp_X]/30mL
  • .3 g/30mL
  • 4 [hp_X]/30mL
  • 12 [hp_X]/30mL
  • .3 g/30mL
  • .3 g/30mL
  • 4 [hp_X]/30mL

Pharmaceutical Classes:

  • Aldosterone Antagonist [EPC]
  • Aldosterone Antagonists [MoA]
  • Allergens [CS]
  • Bee Venoms [CS]
  • Cell-mediated Immunity [PE]
  • Decreased Renal K+ Excretion [PE]
  • Increased Diuresis [PE]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Potassium-sparing Diuretic [EPC]
  • Standardized Insect Venom Allergenic Extract [EPC]
  • Thiazide Diuretic [EPC]
  • Thiazides [CS]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.