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,

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1948

Energy Catalyst also known as 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, is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Energy Catalyst is 43742-1948. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Energy Catalyst drug includes 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 and more. The currest status of Energy Catalyst drug is Active.

Drug Information:

Drug NDC:	43742-1948
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Energy Catalyst
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
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,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	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 Load more... 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 - 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 - 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 URANIUM - 12 [hp_X]/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
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date:	15 Mar, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	23 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	M0022797 N0000175952 N0000185508 N0000175629 N0000184306 M0000728 M0005152 N0000175831 N0000008595 N0000008924 N0000175830
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	E0399OZS9N CPD4NFA903 LMI26O6933 F79059A38U S7V92P67HO 6P669D8HQ8 OW5102UV6N U015TT5I8H SBV4XY874G 00BH33GNGH Load more... 30K4522N6T 0UV74P3R0J GNR9HML8BA 1C6V77QF41 0R0008Q3JB 3G0H8C9362 26SK597UWV 789U1901C5 LRX7AJ16DT 1D4N45714Q 77B218D3YE 444W947O8O R5L488RY0Q AU0V1LM3JT 96WE91N25T 79Y1949PYO W1XX32SQN1 045A6V3VFX 9679TC07X4 44448S9773 E1UOL152H7 6I3K30563S 2P299V784P 9FN79X2M3F I38ZP9992A R17X820ROL 42Z2K6ZL8P 9YY2F980SV 53GH7MZT1R 324Y4038G2 81AH48963U AYT3H319PN 7OV03QG267 99QP4ELX96 05175J654G 2E7M255OPY 5TWQ1V240M 27YLU75U4W 49DFR088MY OC4598NZEQ BQN1B9B9HA NKN7EZA750 56X6LID5ZY DMK383DSAC 93722E7JA1 42OD65L39F H6241UJ22B 3M4G523W1G 451W47IQ8X 948QAQ08I1 YZS2RPE8LE 70FD1KFU70 6424HBN274 06SSF7P179 AD84R52XLF 387GMG9FH5 91D9GV0Z28 4OC371KSTK 00J9J9XKDE BK9092J5MP T66CZ53RP4 J41CSQ7QDS
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Vitamin D [EPC] Standardized Chemical Allergen [EPC] Copper-containing Intrauterine Device [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Inhibit Ovum Fertilization [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Vitamin D [CS] Allergens [CS] Copper [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Blood Coagulation Factor [EPC] Calcium [CS] Calculi Dissolution Agent [EPC] Cations Divalent [CS] Cell-mediated Immunity [PE] Copper [CS] Copper-containing Intrauterine Device [EPC] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Increased Coagulation Factor Activity [PE] Increased Histamine Release [PE] Increased Large Intestinal Motility [PE] Inhibit Ovum Fertilization [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Inhibition Small Intestine Fluid/Electrolyte Absorption [PE] Magnesium Ion Exchange Activity [MoA] Magnetic Resonance Contrast Activity [MoA] Mood Stabilizer [EPC] Osmotic Activity [MoA] Osmotic Laxative [EPC] Paramagnetic Contrast Agent [EPC] Standardized Chemical Allergen [EPC] Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] Vitamin D [CS] Vitamin D [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1948-1	60 mL in 1 BOTTLE, DROPPER (43742-1948-1)	15 Mar, 2021	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Energy Catalyst

Viscum Album & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1948

Purpose:

Homeopathic indications: 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.

Product Elements:

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, viscum album fruiting top viscum album fruiting top cobaltous gluconate cobaltous cation cupric sulfate cupric cation ferrous fumarate ferrous cation magnesium aspartate magnesium cation manganese gluconate manganese cation (2+) phosphorus phosphorus potassium aspartate aspartic acid sodium molybdate molybdate ion adenosine cyclic phosphate adenosine cyclic phosphate cerous oxalate nonahydrate cerous cation nickel acetate nickel cation tribasic calcium phosphate calcium cation chromium chromium cobalt cobalt copper copper iron iron iodine iodine iridium iridium potassium carbonate carbonate ion lithium lithium cation magnesium magnesium manganese manganese molybdenum molybdenum sodium chloride chloride ion selenium selenium strontium strontium sulfur sulfur vanadium vanadium zinc zinc cholecalciferol cholecalciferol aluminum aluminum antimony trisulfide antimony trisulfide silver silver arsenic trioxide arsenic cation (3+) gold gold barium carbonate barium cation beryllium beryllium bismuth bismuth bromine bromine cadmium cadmium cerium cerium cesium chloride cesium cation dysprosium dysprosium erbium erbium europium europium gadolinium gadolinium germanium sesquioxide germanium sesquioxide holmium holmium indium indium mercurius solubilis mercurius solubilis neodymium oxide neodymium oxide nickel nickel osmium osmium palladium palladium platinum platinum lead lead praseodymium praseodymium rhodium rhodium rubidium nitrite rubidium cation nitrite ion samarium samarium tin tin terbium terbium thallium thallium uranium uranium ytterbium oxide ytterbium oxide aluminum oxide aluminum oxide mercuric chloride mercuric cation lanthanum lanthanum niobium niobium tantalum tantalum proteus morganii proteus morganii water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact a physician or poison control center right away. if pregnant or breast-feeding, ask a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing.

Dosage and Administration:

Directions: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1948-1 homeopathic energy catalyst 2 fl oz (60 ml) energy catalyst

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.