43742-0170 : Oratox Oral Liquid


NDC43742-0170
Labeler: Deseret Biologicals, Inc.
Product Type: Human Prescription Drug
Drug Name: Oratox
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 43742-0170-1: 30 ML IN 1 BOTTLE, DROPPER (43742‑0170‑1)

Active Ingredients:

  • Calcium Chloride
  • Copper
  • Eugenol
  • Formaldehyde
  • Fucus Vesiculosus
  • Gold
  • Iodine
  • Lidocaine
  • Mercurius Solubilis
  • Molybdenum
  • Nickel
  • Palladium
  • Selenium
  • Silver
  • Sodium Chloride
  • Sodium Fluoride
  • Sus Scrofa Bone Marrow
  • Sus Scrofa Lymph
  • Sus Scrofa Thymus
  • Sus Scrofa Thyroid
  • Tin
  • Titanium
  • Vanadium
  • Zinc

Dosage Strength:

  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 3 [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
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 8 [hp_X]/mL
  • 8 [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

Pharmaceutical Classes:

  • Blood Coagulation Factor [EPC]
  • Increased Coagulation Factor Activity [PE]
  • Calcium [Chemical/Ingredient]
  • Cations
  • Divalent [Chemical/Ingredient]
  • Standardized Chemical Allergen [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Allergens [Chemical/Ingredient]
  • Copper [Chemical/Ingredient]
  • Copper-containing Intrauterine Device [EPC]
  • Decreased Embryonic Implantation [PE]
  • Decreased Sperm Motility [PE]
  • Inhibit Ovum Fertilization [PE]
  • Amide Local Anesthetic [EPC]
  • Amides [Chemical/Ingredient]
  • Antiarrhythmic [EPC]
  • Local Anesthesia [PE]

Related Products:

Based on records with the same trade name.
  • 43742-0775 Oratox Oral Liquid by Deseret Biologicals, Inc.
  • 43742-0944 Oratox Oral Liquid by Deseret Biologicals, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 43742-0170 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.