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  4. NDC Product Code: 44911-0703 Mitochondria Pro

NDC 44911-0703 Mitochondria Pro

Aralia Quinquefolia,Arnica Montana,Adenosinum Triphosphoricum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0703?
  4. Mitochondria Pro Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
44911-0703
Proprietary Name:
Mitochondria Pro
Non-Proprietary Name: [1]
Aralia Quinquefolia, Arnica Montana, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Ascorbicum Acidum, Alpha-lipoicum Acidum, Calcarea Carbonica, Citricum Acidum, Cuprum Metallicum, Cysteinum, Ferrum Metallicum, Iodium, Levothyroxinum, Magnesium Gluconicum Dihydricum, Malicum Acidum, Manganum Aceticum, Nadidum, Natrum Pyruvicum, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Selenium Metallicum, Sulphur, Thiaminum Hydrochloricum, Ubidecarenonum, Zincum Metallicum,
Substance Name: [2]
Aconitic Acid, (z)-; Adenosine Triphosphate Disodium; Alpha Lipoic Acid; American Ginseng; Anhydrous Citric Acid; Arnica Montana Whole; Arsenic Trioxide; Ascorbic Acid; Barium Oxalosuccinate; Bryonia Alba Root; Cinchona Officinalis Bark; Conium Maculatum Flowering Top; Copper; Cysteine; Gelsemium Sempervirens Root; Iodine; Iron; Levothyroxine; Magnesium Gluconate; Malic Acid; Manganese Acetate Tetrahydrate; Mercurius Solubilis; Nadide; Niacinamide; Oxogluric Acid; Oyster Shell Calcium Carbonate, Crude; Pyridoxine Hydrochloride; Riboflavin; Selenium; Silicon Dioxide; Sodium Pyruvate; Sulfur; Thiamine Hydrochloride; Ubidecarenone; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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 Name: [5]
    Energique, Inc.
    Labeler Code:
    44911
    Product Label ID:
    8c3e961d-bc33-40cd-a282-a4fe5aa3f0ad
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-28-2023
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 44911-0703?

    The NDC code 44911-0703 is assigned by the FDA to the product Mitochondria Pro which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Mitochondria Pro is aralia quinquefolia, arnica montana, adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, ascorbicum acidum, alpha-lipoicum acidum, calcarea carbonica, citricum acidum, cuprum metallicum, cysteinum, ferrum metallicum, iodium, levothyroxinum, magnesium gluconicum dihydricum, malicum acidum, manganum aceticum, nadidum, natrum pyruvicum, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, selenium metallicum, sulphur, thiaminum hydrochloricum, ubidecarenonum, zincum metallicum, . The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 44911-0703-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Mitochondria Pro?

    • Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. • Consult a physician for use in children under 12 years of age.

    What are Mitochondria Pro Active Ingredients?

    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.
    • ACONITIC ACID, (Z)- 16 [hp_X]/mL
    • ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
    • ALPHA LIPOIC ACID 12 [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.
    • AMERICAN GINSENG 6 [hp_X]/mL
    • ANHYDROUS CITRIC ACID 12 [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.
    • ARNICA MONTANA WHOLE 6 [hp_X]/mL
    • ARSENIC TRIOXIDE 30 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
    • ASCORBIC ACID 12 [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 35 [hp_C]/mL
    • BRYONIA ALBA ROOT 30 [hp_X]/mL
    • CINCHONA OFFICINALIS BARK 30 [hp_X]/mL
    • CONIUM MACULATUM FLOWERING TOP 30 [hp_X]/mL
    • COPPER 12 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
    • CYSTEINE 12 [hp_X]/mL - A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
    • GELSEMIUM SEMPERVIRENS ROOT 30 [hp_X]/mL
    • IODINE 12 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
    • IRON 12 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
    • LEVOTHYROXINE 12 [hp_X]/mL
    • MAGNESIUM GLUCONATE 12 [hp_X]/mL
    • MALIC ACID 12 [hp_X]/mL
    • MANGANESE ACETATE TETRAHYDRATE 12 [hp_X]/mL
    • MERCURIUS SOLUBILIS 30 [hp_X]/mL
    • NADIDE 12 [hp_X]/mL
    • NIACINAMIDE 12 [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 12 [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)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
    • PYRIDOXINE HYDROCHLORIDE 12 [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 12 [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.
    • SELENIUM 12 [hp_X]/mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
    • SILICON DIOXIDE 30 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
    • SODIUM PYRUVATE 12 [hp_X]/mL
    • SULFUR 12 [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 12 [hp_X]/mL
    • UBIDECARENONE 12 [hp_X]/mL
    • ZINC 12 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

    Which are Mitochondria Pro UNII Codes?

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

    Which are Mitochondria Pro Inactive Ingredients 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 for Mitochondria Pro?

    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.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".