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  5. NDC Package Code: 43742-0944-1 Oratox

NDC Package 43742-0944-1 Oratox

Fucus Vesiculosus,Lymph Node (suis),Medulla Ossis Suis,Thymus (suis),Thyroidinum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
43742-0944-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-0944
Proprietary Name:
Oratox
Non-Proprietary Name:
Fucus Vesiculosus, Lymph Node (suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis), Calcarea Muriatica, Iodium, Natrum Fluoratum, Natrum Muriaticum, Selenium Metallicum, Vanadium Metallicum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum Metallicum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum
Substance Name:
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
Usage Information:
For temporary relief of symptoms related to heavy metal toxicity caused by toxic dental materials in the mouth. These include muscle cramps, inflammation, and joint pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to heavy metal toxicity caused by toxic dental materials in the mouth. These include muscle cramps, inflammation, and joint pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742094401
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CALCIUM CHLORIDE 12 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • EUGENOL 12 [hp_X]/mL
  • FORMALDEHYDE 12 [hp_X]/mL
  • FUCUS VESICULOSUS 3 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • LIDOCAINE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • SILVER 12 [hp_X]/mL
  • SODIUM CHLORIDE 12 [hp_X]/mL
  • SODIUM FLUORIDE 12 [hp_X]/mL
  • SUS SCROFA BONE MARROW 8 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • TIN 12 [hp_X]/mL
  • TITANIUM 12 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
  • Amides - [CS]
  • Antiarrhythmic - [EPC] (Established Pharmacologic Class)
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
  • Local Anesthesia - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    12-27-2016
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 43742-0944-1?

    The NDC Packaged Code 43742-0944-1 is assigned to a package of 30 ml in 1 bottle, dropper of Oratox, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-0944 included in the NDC Directory?

    Yes, Oratox with product code 43742-0944 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on December 27, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43742-0944-1?

    The 11-digit format is 43742094401. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-143742-0944-15-4-243742-0944-01