Adeps Suillus, Bryonia (alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-methionine, Methylcobalamin, Proteus (vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum Liquid
NDC Package 43742-2330-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Adeps Suillus, Bryonia (alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-methionine, Methylcobalamin, Proteus (vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum liquids is a drug for further processing. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals,inc., this product is identified by NDC 43742-2330.

Identification & Billing

NDC Package Code
43742-2330-1
Package Description
960 mL in 1 CONTAINER
Product Code
43742-2330
11-Digit Billing Format
43742233001

Clinical Specifications

Proprietary Name
Adeps Suillus, Bryonia (alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-methionine, Methylcobalamin, Proteus (vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum
Non-Proprietary Name
Adeps Suillus, Bryonia (alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-methionine, Methylcobalamin, Proteus (vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum
Substance Name
Allylthiourea; Bryonia Alba Root; Choline Hydroxide; Dopamine Hydrochloride; Ferrosoferric Phosphate; Folic Acid; Herring Sperm Dna; Insulin Human; Lard; Leptin Human; Magnesium Chloride; Methionine; Methylcobalamin; Proteus Vulgaris; Riboflavin; Ruta Graveolens Flowering Top; Sucrose; Toxicodendron Pubescens Leaf; Tribasic Calcium Phosphate; Zinc
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.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Deseret Biologicals,inc.
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
04-28-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43742-2330-1 identifies a specific commercial package of 960 ml in 1 container of Adeps Suillus, Bryonia (alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-methionine, Methylcobalamin, Proteus (vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum (UNFINISHED drug), drug for further processing labeled by Deseret Biologicals,inc.. This liquid is formulated for use and contains allylthiourea; bryonia alba root; choline hydroxide; dopamine hydrochloride; ferrosoferric phosphate; folic acid; herring sperm dna; insulin human; lard; leptin human; magnesium chloride; methionine; methylcobalamin; proteus vulgaris; riboflavin; ruta graveolens flowering top; sucrose; toxicodendron pubescens leaf; tribasic calcium phosphate; zinc as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Deseret Biologicals,inc. on April 28, 2026. The current certification is valid through December 31, 2027.

How is this Deseret Biologicals,inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742233001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43742-2330-1
11-Digit CMS (5-4-2)
43742-2330-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.