Energy Catalyst Liquid
NDC Package 43742-2203-1
Package Information
Energy Catalyst (adenosinum cyclophosphoricum, alumina, arsenicum album, cerium oxalicum, cobalt gluconate, cuprum sulphuricum, calcarea phosphorica, chromium metallicum, cobaltum metallicum, cuprum metallicum, ferrum metallicum, iodium, iridium metallicum, kali carbonicum, lithium carbonicum, magnesium metallicum, manganum metallicum, molybdenum, natrum muriaticum, phosphorus, selenium metallicum, strontium carbonicum, sulphur, vanadium metallicum, zincum metallicum, aluminium metallicum, antimonium crudum,) liquids is 1-10 drops under the tongue, 3 times a day or as directed by a health professional. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2203.
Identification & Billing
Clinical Specifications
- ADENOSINE CYCLIC PHOSPHATE 8 [hp_X]/mL
- ALUMINUM 12 [hp_X]/mL
- ALUMINUM OXIDE 30 [hp_X]/mL
- ANTIMONY TRISULFIDE 12 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- BARIUM CARBONATE 12 [hp_X]/mL
- BERYLLIUM 12 [hp_X]/mL
- BISMUTH 12 [hp_X]/mL
- BROMINE 12 [hp_X]/mL
- CADMIUM 12 [hp_X]/mL
- CERIUM 12 [hp_X]/mL
- CEROUS OXALATE NONAHYDRATE 8 [hp_X]/mL
- CESIUM CHLORIDE 12 [hp_X]/mL
- CHOLECALCIFEROL 8 [hp_X]/mL
- CHROMIUM 8 [hp_X]/mL
- COBALT 8 [hp_X]/mL
- COBALTOUS GLUCONATE 6 [hp_X]/mL
- COPPER 8 [hp_X]/mL
- CUPRIC SULFATE 6 [hp_X]/mL
- DYSPROSIUM 12 [hp_X]/mL
- ERBIUM 12 [hp_X]/mL
- EUROPIUM 12 [hp_X]/mL
- FERROUS FUMARATE 6 [hp_X]/mL
- GADOLINIUM 12 [hp_X]/mL
- GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
- GOLD 12 [hp_X]/mL
- HOLMIUM 12 [hp_X]/mL
- INDIUM 12 [hp_X]/mL
- IODINE 8 [hp_X]/mL
- IRIDIUM 8 [hp_X]/mL
- IRON 8 [hp_X]/mL
- LANTHANUM 14 [hp_C]/mL
- LEAD 12 [hp_X]/mL
- LITHIUM CARBONATE 8 [hp_X]/mL
- MAGNESIUM 8 [hp_X]/mL
- MAGNESIUM ASPARTATE 6 [hp_X]/mL
- MANGANESE 8 [hp_X]/mL
- MANGANESE GLUCONATE 6 [hp_X]/mL
- MERCURIC CHLORIDE 30 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- MOLYBDENUM 8 [hp_X]/mL
- NEODYMIUM OXIDE 12 [hp_X]/mL
- NICKEL 12 [hp_X]/mL
- NICKEL ACETATE 8 [hp_X]/mL
- NIOBIUM 30 [hp_C]/mL
- OSMIUM 12 [hp_X]/mL
- PALLADIUM 12 [hp_X]/mL
- PHOSPHORUS 6 [hp_X]/mL
- PLATINUM 12 [hp_X]/mL
- POTASSIUM ASPARTATE 6 [hp_X]/mL
- POTASSIUM CARBONATE 8 [hp_X]/mL
- PRASEODYMIUM 12 [hp_X]/mL
- PROTEUS MORGANII 30 [hp_C]/mL
- RHODIUM 12 [hp_X]/mL
- RUBIDIUM NITRITE 12 [hp_X]/mL
- SAMARIUM 12 [hp_X]/mL
- SELENIUM 8 [hp_X]/mL
- SILVER 12 [hp_X]/mL
- SODIUM CHLORIDE 8 [hp_X]/mL
- SODIUM MOLYBDATE 6 [hp_X]/mL
- STRONTIUM CARBONATE 8 [hp_X]/mL
- SULFUR 8 [hp_X]/mL
- TANTALUM 30 [hp_C]/mL
- TERBIUM 12 [hp_X]/mL
- THALLIUM 12 [hp_X]/mL
- TIN 12 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 8 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 15 [hp_C]/mL
- VANADIUM 8 [hp_X]/mL
- VISCUM ALBUM FRUITING TOP 3 [hp_X]/mL
- YTTERBIUM OXIDE 12 [hp_X]/mL
- ZINC 8 [hp_X]/mL
- Allergens - [CS]
- Allergens - [CS]
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- 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)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
- Mood Stabilizer - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
- Vitamin D - [CS]
- Vitamin D - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-2203 - Energy Catalyst
- 43742-2203-1 - 60 mL in 1 BOTTLE, DROPPER
- 43742-2203 - Energy Catalyst
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 43742-2203-1 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 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 carbonate; 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 carbonate; sulfur; tantalum; terbium; thallium; tin; tribasic calcium phosphate; uranyl nitrate hexahydrate; vanadium; viscum album fruiting top; ytterbium oxide; 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 December 10, 2024. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742220301. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.