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  5. NDC Package Code: 43742-0756-1 Energy Catalyst

NDC Package 43742-0756-1 Energy Catalyst

Viscum Album,Cobalt Gluconate,Cuprum Sulphuricum,Ferrous Fumarate,Magnesium - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
43742-0756-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-0756
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
Substance Name:
Adenosine Cyclic Phosphate; Aluminum; Aluminum Oxide; Antimony Trisulfide; Arsenic Trioxide; Barium Carbonate; Beryllium; Bismuth; Bromine; Cadmium; Cerium; Cerous Oxalate Nonahydrate; Cesium Chloride; Cholecalciferol; Chromium; Cobalt; Cobaltous Gluconate; Copper; Cupric Sulfate; Dysprosium; Erbium; Europium; Ferrous Fumarate; Gadolinium; Germanium Sesquioxide; Gold; Holmium; Indium; Iodine; Iridium; Iron; Lanthanum; Lead; Lithium; Magnesium; Magnesium Aspartate; Manganese; Manganese Gluconate; Mercuric Chloride; Mercurius Solubilis; Molybdenum; Neodymium Oxide; Nickel; Nickel Acetate; Niobium; Osmium; Palladium; Phosphorus; Platinum; Potassium Aspartate; Potassium Carbonate; Praseodymium; Proteus Morganii; Rhodium; Rubidium Nitrite; Samarium; Selenium; Silver; Sodium Chloride; Sodium Molybdate; Strontium; Sulfur; Tantalum; Terbium; Thallium; Tin; Tribasic Calcium Phosphate; Uranium; Vanadium; Viscum Album Fruiting Top; Ytterbium Oxide; Zinc
Usage Information:
For temporary relief of symptoms related to mineral imbalance in the body including fatigue, dehydration, nervousness and cramping pains.****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 mineral imbalance in the body including fatigue, dehydration, nervousness and cramping pains.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742075601
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):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
06-02-2016
End Marketing Date:
08-31-2025
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 43742-0756-1?

The NDC Packaged Code 43742-0756-1 is assigned to a package of 30 ml in 1 bottle, dropper of Energy Catalyst, 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 43742-0756 included in the NDC Directory?

Yes, Energy Catalyst with product code 43742-0756 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on June 02, 2016.

What is the 11-digit format for NDC 43742-0756-1?

The 11-digit format is 43742075601. 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
5-4-143742-0756-15-4-243742-0756-01