NDC 43742-0586 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, Vitamin D3, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum

NDC Product Code 43742-0586

NDC Code: 43742-0586

Proprietary Name: Energy Catalyst What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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, Vitamin D3, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.


Code Structure
  • 43742 - Deseret Biologicals, Inc.
    • 43742-0586 - Energy Catalyst

NDC 43742-0586-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Energy Catalyst with NDC 43742-0586 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Energy Catalyst is viscum album, cobalt gluconate, cuprum sulphuricum, ferrous fumarate, magnesium aspartate, manganese gluconate, phosphorus, potassium aspartate, sodium molybdate, adenosinum cyclophosphoricum, cerium oxalicum, nickel acetate, vitamin d3, aluminium metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium, cadmium metallicum, cerium metallicum, cesium chloride, chromium, cobaltum metallicum. The product's dosage form is liquid and is administered via oral form.

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Energy Catalyst Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • VISCUM ALBUM FRUITING TOP 3 [hp_X]/mL
  • COBALTOUS GLUCONATE 6 [hp_X]/mL
  • CUPRIC SULFATE 6 [hp_X]/mL
  • FERROUS FUMARATE 6 [hp_X]/mL
  • MAGNESIUM ASPARTATE 6 [hp_X]/mL
  • MANGANESE GLUCONATE 6 [hp_X]/mL
  • PHOSPHORUS 6 [hp_X]/mL
  • POTASSIUM ASPARTATE 6 [hp_X]/mL
  • SODIUM MOLYBDATE 6 [hp_X]/mL
  • ADENOSINE CYCLIC PHOSPHATE 8 [hp_X]/mL
  • CEROUS OXALATE NONAHYDRATE 8 [hp_X]/mL
  • NICKEL ACETATE 8 [hp_X]/mL
  • CHOLECALCIFEROL 8 [hp_X]/mL
  • ALUMINUM 12 [hp_X]/mL
  • ANTIMONY TRISULFIDE 12 [hp_X]/mL
  • SILVER 12 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • BARIUM CARBONATE 12 [hp_X]/mL
  • BERYLLIUM 12 [hp_X]/mL
  • BISMUTH 12 [hp_X]/mL
  • BORON 12 [hp_X]/mL
  • BROMINE 12 [hp_X]/mL
  • CADMIUM 12 [hp_X]/mL
  • CERIUM 12 [hp_X]/mL
  • CESIUM CHLORIDE 12 [hp_X]/mL
  • CHROMIUM 12 [hp_X]/mL
  • COBALT 12 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • DYSPROSIUM 12 [hp_X]/mL
  • ERBIUM 12 [hp_X]/mL
  • EUROPIUM 12 [hp_X]/mL
  • IRON 12 [hp_X]/mL
  • GADOLINIUM 12 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
  • HOLMIUM 12 [hp_X]/mL
  • INDIUM 12 [hp_X]/mL
  • LITHIUM 12 [hp_X]/mL
  • MAGNESIUM 12 [hp_X]/mL
  • MANGANESE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • NEODYMIUM OXIDE 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • OSMIUM 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • PLATINUM 12 [hp_X]/mL
  • LEAD 12 [hp_X]/mL
  • PRASEODYMIUM 12 [hp_X]/mL
  • RHODIUM 12 [hp_X]/mL
  • RUBIDIUM NITRITE 12 [hp_X]/mL
  • SAMARIUM 12 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • TIN 12 [hp_X]/mL
  • STRONTIUM CARBONATE 12 [hp_X]/mL
  • TERBIUM 12 [hp_X]/mL
  • THALLIUM 12 [hp_X]/mL
  • URANIUM 12 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL
  • YTTERBIUM OXIDE 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL
  • ALUMINUM OXIDE 30 [hp_X]/mL
  • MERCURIC CHLORIDE 30 [hp_X]/mL
  • LANTHANUM 14 [hp_C]/mL
  • NIOBIUM 30 [hp_C]/mL
  • TANTALUM 30 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 07-21-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 11-09-2020 What is the End Marketing Date?
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.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Energy Catalyst Product Label Images

Energy Catalyst Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Viscum Album 3X, 30X, 200X, Cobalt Gluconate 6X, Cuprum Sulphuricum 6X, Ferrous Fumarate 6X, Magnesium Aspartate 6X, Manganese Gluconate 6X, Phosphorus 6X, Potassium Aspartate 6X, Sodium Molybdate 6X, Adenosinum Cyclophosphoricum 8X, Cerium Oxalicum 8X, Nickel Acetate 8X, Vitamin D3 8X, 30X, 200X, Aluminium Metallicum 12X, 30X, Antimonium Crudum 12X, 30X, Argentum Metallicum 12X, 30X, Arsenicum Album 12X, 30X, Aurum Metallicum 12X, 30X, Baryta Carbonica 12X, 30X, Beryllium Metallicum 12X, 30X, Bismuthum Metallicum 12X, 30X, Boron 12X, 30X, Bromium 12X, 30X, Cadmium Metallicum 12X, 30X, Cerium Metallicum 12X, 30X, Cesium Chloride 12X, 30X, Chromium 12X, 30X, Cobaltum Metallicum 12X, 30X, Cuprum Metallicum 12X, 30X, Dysprosium Metallicum 12X, 30X, Erbium Metallicum 12X, 30X, Europium Metallicum 12X, 30X, Ferrum Metallicum 12X, 30X, Gadolinium Metallicum 12X, 30X, Germanium Sesquioxide 12X, 30X, Holmium Metallicum 12X, 30X, Indium Metallicum 12X, 30X, Lithium Carbonicum 12X, 30X, Magnesium Metallicum 12X, 30X, Manganum Metallicum 12X, 30X, Mercurius Solubilis 12X, 30X, Molybdenum 12X, 30X, Neodymium Oxide 12X, 30X, Niccolum Metallicum 12X, 30X, Osmium Metallicum 12X, 30X, Palladium Metallicum 12X, 30X, Platinum Metallicum 12X, 30X, Plumbum Metallicum 12X, 30X, Praseodymium Metallicum 12X, 30X, Rhodium Metallicum 12X, 30X, Rubidium Nitricum 12X, 30X, Samarium Metallicum 12X, 30X, Selenium Metallicum 12X, 30, Stannum Metallicum 12X, 30X, Strontium Carbonicum 12X, 30X, Terbium Metallicum 12X, 30X, Thallium Metallicum 12X, 30X, Uranium Nitricum 12X, 30X, Vanadium Metallicum 12X, 30X, Ytterbium Oxide 12X, 30X, Zincum Metallicum 12X, 30X, Alumina 30X, 200X, Mercurius Corrosivus 30X, 200X, Plumbum Metallicum 200X, Lanthanum Metallicum 14C, Niobium Metallicum 30C, Tantalum Metallicum 30C, Morgan Bacillus (Pure) 30C, 200C.

Indications:

For temporary relief of symptoms related to mineral imbalance in the body including fatigue, dehydration, 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, dehydration, nervousness and cramping pains.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

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.

Inactive Ingredients:

Demineralized Water, 25% Ethanol.

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com**For a complete list of Heavy Metal Isodes contact Deseret Biologicals, Inc.

Package Label Display:

DESBIONDC 43742-0586-1HOMEOPATHICENERGYCATALYST1 FL OZ (30 ML)

* Please review the disclaimer below.

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