Bio Co-enzyme Phase Liquid
NDC 43742-1661

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1661?
  4. Bio Co-enzyme Phase Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Bio Co-enzyme Phase (beta vulgaris, ascorbicum acidum, cysteinum, natrum oxalaceticum, nicotinamidum, pulsatilla (pratensis), pyridoxinum hydrochloricum, riboflavinum, thiaminum hydrochloricum, alpha-ketoglutaricum acidum, alpha-lipoicum acidum, cerium oxalicum, citricum acidum, fumaricum acidum, magnesium oroticum dihydricum, malicum acidum, nadidum, natrum pyruvicum, pantothenic acid, succinicum acidum, adrenalinum, adenosinum triphosphoricum dinatrum, hepar sulphuris calcareum, sulphur, aconiticum acidum, cis-,) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a acidifying activity [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1661 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-1661
Proprietary Name:
Bio Co-enzyme Phase
Non-Proprietary Name: [1]
Beta Vulgaris, Ascorbicum Acidum, Cysteinum, Natrum Oxalaceticum, Nicotinamidum, Pulsatilla (pratensis), Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-ketoglutaricum Acidum, Alpha-lipoicum Acidum, Cerium Oxalicum, Citricum Acidum, Fumaricum Acidum, Magnesium Oroticum Dihydricum, Malicum Acidum, Nadidum, Natrum Pyruvicum, Pantothenic Acid, Succinicum Acidum, Adrenalinum, Adenosinum Triphosphoricum Dinatrum, Hepar Sulphuris Calcareum, Sulphur, Aconiticum Acidum, Cis-,
Substance Name: [2]
Acetic Acid; Adenosine Triphosphate Disodium; Alpha Lipoic Acid; Anhydrous Citric Acid; Ascorbic Acid; Barium Oxalosuccinate; Beta Vulgaris Whole; Calcium Sulfide; Cerous Oxalate Nonahydrate; Cysteine; Epinephrine; Fumaric Acid; Magnesium Orotate Dihydrate; Malic Acid; Manganese Phosphate, Dibasic; Nadide; Niacinamide; Oxogluric Acid; Pantothenic Acid; Proteus Morganii; Pulsatilla Pratensis Whole; Pyridoxine Hydrochloride; Riboflavin; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Succinic Acid; Sulfur; Thiamine Hydrochloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
e8f6e2ec-ae2e-4bee-b9d3-5f3a2e3daf65
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
06-08-2020
End Marketing Date: [10]
10-15-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-1661?

The NDC code 43742-1661 is assigned by the FDA to the product Bio Co-enzyme Phase. It is commonly known by its generic name, beta vulgaris, ascorbicum acidum, cysteinum, natrum oxalaceticum, nicotinamidum, pulsatilla (pratensis), pyridoxinum hydrochloricum, riboflavinum, thiaminum hydrochloricum, alpha-ketoglutaricum acidum, alpha-lipoicum acidum, cerium oxalicum, citricum acidum, fumaricum acidum, magnesium oroticum dihydricum, malicum acidum, nadidum, natrum pyruvicum, pantothenic acid, succinicum acidum, adrenalinum, adenosinum triphosphoricum dinatrum, hepar sulphuris calcareum, sulphur, aconiticum acidum, cis-, . This pharmaceutical product is labeled by Deseret Biologicals, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-1661-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

For the temporary relief of exhaustion, fatigue, and feelings of low energy.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of exhaustion, fatigue, and feelings of low energy.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

What are Active Ingredients of this product?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ACETIC ACID 16 [hp_X]/mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
  • ADENOSINE TRIPHOSPHATE DISODIUM 10 [hp_X]/mL
  • ALPHA LIPOIC ACID 8 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
  • ANHYDROUS CITRIC ACID 8 [hp_X]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
  • ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • BARIUM OXALOSUCCINATE 34 [hp_C]/mL
  • BETA VULGARIS WHOLE 4 [hp_X]/mL
  • CALCIUM SULFIDE 10 [hp_X]/mL - RN given refers to parent cpd; see also record for lime sulfur (calcium polysulfide)
  • CEROUS OXALATE NONAHYDRATE 8 [hp_X]/mL
  • CYSTEINE 6 [hp_X]/mL - A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
  • EPINEPHRINE 8 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
  • FUMARIC ACID 8 [hp_X]/mL - see also record for ferrous fumarate; use FUMARATES for general fumaric acid esters
  • MAGNESIUM OROTATE DIHYDRATE 8 [hp_X]/mL
  • MALIC ACID 8 [hp_X]/mL
  • MANGANESE PHOSPHATE, DIBASIC 16 [hp_X]/mL
  • NADIDE 8 [hp_X]/mL
  • NIACINAMIDE 6 [hp_X]/mL - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
  • OXOGLURIC ACID 8 [hp_X]/mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
  • PANTOTHENIC ACID 8 [hp_X]/mL - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
  • PROTEUS MORGANII 30 [hp_C]/mL
  • PULSATILLA PRATENSIS WHOLE 6 [hp_X]/mL
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
  • RIBOFLAVIN 6 [hp_X]/mL - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
  • SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
  • SODIUM PYRUVATE 8 [hp_X]/mL
  • SUCCINIC ACID 8 [hp_X]/mL - A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
  • SULFUR 10 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
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.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".