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  4. NDC Product Code: 44911-0451 Recovatone

NDC 44911-0451 Recovatone

Glycyrrhiza Glabra,Kali Muriaticum,Zincum Gluconicum,Kali - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0451?
  4. Recovatone Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
44911-0451
Proprietary Name:
Recovatone
Non-Proprietary Name: [1]
Glycyrrhiza Glabra, Kali Muriaticum, Zincum Gluconicum, Kali Phosphoricum, Iodium, Phosphorus, Adrenocorticotrophin, Ascorbicum Acidum, Calcium Gluconate, L-arginine, L-carnitine, L-ornithine, Magnesia Muriatica, Magnesium Gluconicum, Dihydricum, Manganese Gluconate, Natrum Muriaticum, Adrenalinum, Cobalt Gluconate, Copper Gluconate, Creatine, Ferrous Gluconate, Glutamine, L-leucine, L-valine, Potassium Gluconate, Selenium Dioxide, Boron, Calcarea Phosphorica, Chromium, Molybdenum, Niccolum Metallicum
Substance Name: [2]
Arginine; Ascorbic Acid; Boron; Calcium Gluconate; Carnitine; Chromium; Cobaltous Gluconate; Copper Gluconate; Corticotropin; Creatine; Dibasic Potassium Phosphate; Epinephrine; Ferrous Gluconate; Glutamine; Glycyrrhiza Glabra; Iodine; Leucine; Magnesium Chloride; Magnesium Gluconate; Manganese Gluconate; Molybdenum; Nickel; Ornithine; Phosphorus; Potassium Chloride; Potassium Gluconate; Selenium; Selenium Dioxide; Sodium Chloride; Strontium Carbonate; Tribasic Calcium Phosphate; Valine; Vanadium; Zinc Gluconate
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:
    99d752b4-22f4-4fe7-8a72-1bc47ef15c3a
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    04-02-2018
    End Marketing Date: [10]
    09-17-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 44911-0451-1

    Package Description: 120 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 44911-0451?

    The NDC code 44911-0451 is assigned by the FDA to the product Recovatone which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Recovatone is glycyrrhiza glabra, kali muriaticum, zincum gluconicum, kali phosphoricum, iodium, phosphorus, adrenocorticotrophin, ascorbicum acidum, calcium gluconate, l-arginine, l-carnitine, l-ornithine, magnesia muriatica, magnesium gluconicum, dihydricum, manganese gluconate, natrum muriaticum, adrenalinum, cobalt gluconate, copper gluconate, creatine, ferrous gluconate, glutamine, l-leucine, l-valine, potassium gluconate, selenium dioxide, boron, calcarea phosphorica, chromium, molybdenum, niccolum 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 44911-0451-1 120 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 Recovatone?

    May temporarily relieve symptoms associated with exertions, such as muscle pain, muscle weakness, trembling of limbs, and cramps.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with exertions, such as muscle pain, muscle weakness, trembling of limbs, and cramps.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

    What are Recovatone 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.
    • ARGININE 6 [hp_X]/mL - An essential amino acid that is physiologically active in the L-form.
    • 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.
    • BORON 12 [hp_X]/mL - A trace element with the atomic symbol B, atomic number 5, and atomic weight [10.806; 10.821]. Boron-10, an isotope of boron, is used as a neutron absorber in BORON NEUTRON CAPTURE THERAPY.
    • CALCIUM GLUCONATE 6 [hp_X]/mL - The calcium salt of gluconic acid. The compound has a variety of uses, including its use as a calcium replenisher in hypocalcemic states.
    • CARNITINE 6 [hp_X]/mL - A constituent of STRIATED MUSCLE and LIVER. It is an amino acid derivative and an essential cofactor for fatty acid metabolism.
    • CHROMIUM 14 [hp_X]/mL - A trace element that plays a role in glucose metabolism. It has the atomic symbol Cr, atomic number 24, and atomic weight 52. According to the Fourth Annual Report on Carcinogens (NTP85-002,1985), chromium and some of its compounds have been listed as known carcinogens.
    • COBALTOUS GLUCONATE 8 [hp_X]/mL
    • COPPER GLUCONATE 8 [hp_X]/mL - Derivatives of gluconic acid (the structural formula HOCH2(CHOH)4COOH), including its salts and esters.
    • CORTICOTROPIN 6 [hp_X]/mL
    • CREATINE 8 [hp_X]/mL - An amino acid that occurs in vertebrate tissues and in urine. In muscle tissue, creatine generally occurs as phosphocreatine. Creatine is excreted as CREATININE in the urine.
    • DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL
    • 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.
    • FERROUS GLUCONATE 10 [hp_X]/mL
    • GLUTAMINE 8 [hp_X]/mL - A non-essential amino acid present abundantly throughout the body and is involved in many metabolic processes. It is synthesized from GLUTAMIC ACID and AMMONIA. It is the principal carrier of NITROGEN in the body and is an important energy source for many cells.
    • GLYCYRRHIZA GLABRA 1 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
    • IODINE 4 [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.
    • LEUCINE 8 [hp_X]/mL - An essential branched-chain amino acid important for hemoglobin formation.
    • MAGNESIUM CHLORIDE 6 [hp_X]/mL - Magnesium chloride. An inorganic compound consisting of one magnesium and two chloride ions. The compound is used in medicine as a source of magnesium ions, which are essential for many cellular activities. It has also been used as a cathartic and in alloys.
    • MAGNESIUM GLUCONATE 6 [hp_X]/mL
    • MANGANESE GLUCONATE 6 [hp_X]/mL
    • MOLYBDENUM 12 [hp_X]/mL - A metallic element with the atomic symbol Mo, atomic number 42, and atomic weight 95.95. It is an essential trace element, being a component of the enzymes xanthine oxidase, aldehyde oxidase, and nitrate reductase.
    • NICKEL 12 [hp_X]/mL - A trace element with the atomic symbol Ni, atomic number 28, and atomic weight 58.69. It is a cofactor of the enzyme UREASE.
    • ORNITHINE 6 [hp_X]/mL - An amino acid produced in the urea cycle by the splitting off of urea from arginine.
    • PHOSPHORUS 5 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
    • POTASSIUM CHLORIDE 2 [hp_X]/mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
    • POTASSIUM GLUCONATE 8 [hp_X]/mL
    • 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.
    • SELENIUM DIOXIDE 8 [hp_X]/mL - Inorganic compounds formed through the oxidation of selenium.
    • SODIUM CHLORIDE 6 [hp_X]/mL - A ubiquitous sodium salt that is commonly used to season food.
    • STRONTIUM CARBONATE 12 [hp_X]/mL
    • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
    • VALINE 8 [hp_X]/mL - A branched-chain essential amino acid that has stimulant activity. It promotes muscle growth and tissue repair. It is a precursor in the penicillin biosynthetic pathway.
    • VANADIUM 12 [hp_X]/mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.
    • ZINC GLUCONATE 4 [hp_X]/mL

    Which are Recovatone UNII Codes?

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

    Which are Recovatone 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 Recovatone?

    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.

    [10] 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.

    [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".