17089-501 : Guna Female Support Oral Solution/ Drops


NDC17089-501
Labeler: Guna Spa
Product Type: Human OTC Drug
Drug Name: Guna Female Support
Dosage Form: Oral Solution/ Drops
Rev. Date: 


NDC Package Codes:

  • 17089-501-18: 1 BOTTLE, DROPPER IN 1 BOX (17089‑501‑18) > 30 ML IN 1 BOTTLE, DROPPER

Active Ingredients:

  • Lilium Lancifolium Whole Flowering
  • Sus Scrofa Ovary
  • Sepia Officinalis Juice
  • Adenosine Cyclic Phosphate
  • Sus Scrofa Pituitary Gland
  • Sus Scrofa Hypothalamus
  • Sus Scrofa Adrenal Gland
  • Sus Scrofa Pancreas
  • Magnesium Phosphate
  • Dibasic Trihydrate
  • Pulsatilla Vulgaris

Dosage Strength:

  • 6 [hp_X]/30mL
  • 6 [hp_X]/30mL
  • 10 [hp_X]/30mL
  • 6 [hp_X]/30mL
  • 30 [hp_X]/30mL
  • 30 [hp_X]/30mL
  • 30 [hp_X]/30mL
  • 30 [hp_X]/30mL
  • 10 [hp_X]/30mL
  • 8 [hp_X]/30mL

Pharmaceutical Classes:

  • Calculi Dissolution Agent [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • 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.