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  5. NDC Package Code: 43742-1170-1 Progenite

NDC Package 43742-1170-1 Progenite

Ammonium Carbonicum,Baryta Muriatica,Borax,Caulophyllum Thalictroides,Natrum - 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:
43742-1170-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1170
Proprietary Name:
Progenite
Non-Proprietary Name:
Ammonium Carbonicum, Baryta Muriatica, Borax, Caulophyllum Thalictroides, Natrum Carbonicum, Sabal Serrulata, Sabina, Sulphuricum Acidum, Thiosinaminum, Folliculinum, Tuba Uterina Suis, Uterus Suis, Hypothalamus (suis), Thyroidinum (suis), Agnus Castus, Conium Maculatum, Graphites, Hyoscyamus Niger, Sepia, Selenium Metallicum, X-ray
Substance Name:
Alcohol, X-ray Exposed (1000 Rad); Allylthiourea; Ammonium Carbonate; Barium Chloride Dihydrate; Caulophyllum Thalictroides Root; Chaste Tree; Conium Maculatum Flowering Top; Estrone; Graphite; Hyoscyamus Niger; Juniperus Sabina Leafy Twig; Saw Palmetto; Selenium; Sepia Officinalis Juice; Sodium Borate; Sodium Carbonate; Sulfuric Acid; Sus Scrofa Fallopian Tube; Sus Scrofa Hypothalamus; Sus Scrofa Uterus; Thyroid
Usage Information:
For temporary relief of symptoms related to impaired reproductive activity in both males and females, such as hormonal imbalances, reduced sex drive, and irregular menses.****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 impaired reproductive activity in both males and females, such as hormonal imbalances, reduced sex drive, and irregular menses.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742117001
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals
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):
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) 12 [hp_X]/mL
  • ALLYLTHIOUREA 6 [hp_X]/mL
  • AMMONIUM CARBONATE 6 [hp_X]/mL
  • BARIUM CHLORIDE DIHYDRATE 6 [hp_X]/mL
  • CAULOPHYLLUM THALICTROIDES ROOT 6 [hp_X]/mL
  • CHASTE TREE 12 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
  • ESTRONE 6 [hp_X]/mL
  • GRAPHITE 12 [hp_X]/mL
  • HYOSCYAMUS NIGER 12 [hp_X]/mL
  • JUNIPERUS SABINA LEAFY TWIG 6 [hp_X]/mL
  • SAW PALMETTO 6 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • SODIUM BORATE 6 [hp_X]/mL
  • SODIUM CARBONATE 6 [hp_X]/mL
  • SULFURIC ACID 6 [hp_X]/mL
  • SUS SCROFA FALLOPIAN TUBE 6 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • SUS SCROFA UTERUS 6 [hp_X]/mL
  • THYROID 8 [hp_X]/mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-19-2018
    End Marketing Date:
    06-01-2028
    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 43742-1170-1?

    The NDC Packaged Code 43742-1170-1 is assigned to a package of 30 ml in 1 bottle, dropper of Progenite, a human over the counter drug labeled by Deseret Biologicals. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-1170 included in the NDC Directory?

    Yes, Progenite with product code 43742-1170 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals on February 19, 2018.

    What is the 11-digit format for NDC 43742-1170-1?

    The 11-digit format is 43742117001. 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
    5-4-143742-1170-15-4-243742-1170-01