17089-290 : Guna-pms Oral Solution/ Drops


NDC: 17089-290
Labeler: Guna Spa
Product Type: Human OTC Drug
Drug Name: Guna-pms
Dosage Form: Oral Solution/ Drops
Rev. Date: 


NDC Package Codes:

  • 17089-290-18: 1 BOTTLE, DROPPER IN 1 BOX (17089‑290‑18) > 30 ML IN 1 BOTTLE, DROPPER

Active Ingredients:

  • Arsenic Trioxide
  • Estradiol
  • Goldenseal
  • Lachesis Muta Venom
  • Magnesium Phosphate
  • Matricaria Recutita
  • Melatonin
  • Progesterone
  • Strychnos Nux-vomica Seed
  • Sulfur
  • Sus Scrofa Ovary
  • Sus Scrofa Pituitary Gland

Dosage Strength:

  • 6 [hp_C]/30mL
  • 6 [hp_X]/30mL
  • 6 [hp_C]/30mL
  • 4 [hp_C]/30mL
  • 6 [hp_C]/30mL
  • 6 [hp_C]/30mL
  • 4 [hp_C]/30mL
  • 6 [hp_X]/30mL
  • 6 [hp_C]/30mL
  • 6 [hp_C]/30mL
  • 8 [hp_X]/30mL
  • 8 [hp_X]/30mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Calculi Dissolution Agent [EPC]
  • Cell-mediated Immunity [PE]
  • Estradiol Congeners [CS]
  • Estrogen Receptor Agonists [MoA]
  • Estrogen [EPC]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Plant Proteins [CS]
  • Progesterone [CS]
  • Progesterone [EPC]
  • Seed Storage Proteins [CS]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

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.