43742-1170 : Progenite Oral Liquid


NDC43742-1170
Labeler: Deseret Biologicals
Product Type: Human OTC Drug
Drug Name: Progenite
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 43742-1170-1: 30 ML IN 1 BOTTLE, DROPPER (43742‑1170‑1)

Active Ingredients:

  • Ammonium Carbonate
  • Barium Chloride Dihydrate
  • Sodium Borate
  • Caulophyllum Thalictroides Root
  • Sodium Carbonate
  • Saw Palmetto
  • Juniperus Sabina Leafy Twig
  • Sulfuric Acid
  • Allylthiourea
  • Estrone
  • Sus Scrofa Fallopian Tube
  • Sus Scrofa Uterus
  • Sus Scrofa Hypothalamus
  • Thyroid
  • Porcine
  • Chaste Tree
  • Conium Maculatum Flowering Top
  • Graphite
  • Hyoscyamus Niger
  • Sepia Officinalis Juice
  • Selenium
  • Alcohol
  • X-ray Exposed (1000 Rad)

Dosage Strength:

  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 8 [hp_X]/mL
  • 8 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL

Related Products:

Based on records with the same trade name.
  • 43742-2126 Progenite Oral Liquid by Deseret Biologicals

NDC QR Code

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NDC 43742-1170 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.