Energy Catalyst Liquid
NDC Package 43742-1948-1

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

Package Information

Energy Catalyst (viscum album, cobalt gluconate, cuprum sulphuricum, ferrous fumarate, magnesium aspartate, manganese gluconate, phosphorus, potassium aspartate, sodium molybdate, adenosinum, cyclophosphoricum, cerium oxalicum, nickel acetate, aluminium metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, bromium, cadmium metallicum, cerium metallicum, cesium chloride, dysprosium metallicum, erbium metallicum, alumina,) liquids is for temporary relief of symptoms related to mineral imbalance in the body including fatigue, nervousness and cramping pains.****These statements are based upon homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1948.

Identification & Billing

NDC Package Code
43742-1948-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
43742-1948
11-Digit Billing Format
43742194801

Clinical Specifications

Proprietary Name
Energy Catalyst
Non-Proprietary Name
Viscum Album, Cobalt Gluconate, Cuprum Sulphuricum, Ferrous Fumarate, Magnesium Aspartate, Manganese Gluconate, Phosphorus, Potassium Aspartate, Sodium Molybdate, Adenosinum, Cyclophosphoricum, Cerium Oxalicum, Nickel Acetate, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Dysprosium Metallicum, Erbium Metallicum, Alumina,
Substance Name
Viscum Album Fruiting Top; Cobaltous Gluconate; Cupric Sulfate; Ferrous Fumarate; Magnesium Aspartate; Manganese Gluconate; Phosphorus; Potassium Aspartate; Sodium Molybdate; Adenosine Cyclic Phosphate; Cerous Oxalate Nonahydrate; Nickel Acetate; Tribasic Calcium Phosphate; Chromium; Cobalt; Copper; Iron; Iodine; Iridium; Potassium Carbonate; Lithium; Magnesium; Manganese; Molybdenum; Sodium Chloride; Selenium; Strontium; Sulfur; Vanadium; Zinc; Cholecalciferol; Aluminum; Antimony Trisulfide; Silver; Arsenic Trioxide; Gold; Barium Carbonate; Beryllium; Bismuth; Bromine; Cadmium; Cerium; Cesium Chloride; Dysprosium; Erbium; Europium; Gadolinium; Germanium Sesquioxide; Holmium; Indium; Mercurius Solubilis; Neodymium Oxide; Nickel; Osmium; Palladium; Platinum; Lead; Praseodymium; Rhodium; Rubidium Nitrite; Samarium; Tin; Terbium; Thallium; Uranium; Ytterbium Oxide; Aluminum Oxide; Mercuric Chloride; Lanthanum; Niobium; Tantalum; Proteus Morganii
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For temporary relief of symptoms related to mineral imbalance in the body including fatigue, nervousness and cramping pains.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to mineral imbalance in the body including fatigue, nervousness and cramping pains.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Deseret Biologicals, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-15-2021
End Marketing Date
12-28-2028
Exclude Flag
N
Sample Package
No

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 43742-1948-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Energy Catalyst, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains viscum album fruiting top; cobaltous gluconate; cupric sulfate; ferrous fumarate; magnesium aspartate; manganese gluconate; phosphorus; potassium aspartate; sodium molybdate; adenosine cyclic phosphate; cerous oxalate nonahydrate; nickel acetate; tribasic calcium phosphate; chromium; cobalt; copper; iron; iodine; iridium; potassium carbonate; lithium; magnesium; manganese; molybdenum; sodium chloride; selenium; strontium; sulfur; vanadium; zinc; cholecalciferol; aluminum; antimony trisulfide; silver; arsenic trioxide; gold; barium carbonate; beryllium; bismuth; bromine; cadmium; cerium; cesium chloride; dysprosium; erbium; europium; gadolinium; germanium sesquioxide; holmium; indium; mercurius solubilis; neodymium oxide; nickel; osmium; palladium; platinum; lead; praseodymium; rhodium; rubidium nitrite; samarium; tin; terbium; thallium; uranium; ytterbium oxide; aluminum oxide; mercuric chloride; lanthanum; niobium; tantalum; proteus morganii 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 March 15, 2021.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742194801. 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)
43742-1948-1
11-Digit CMS (5-4-2)
43742-1948-01

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