NDC 44911-0734 Recovatone

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

Product Information

Get all the details for National Drug Code (NDC) 44911-0734 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
44911-0734
Proprietary Name:
Recovatone
Non-Proprietary Name: [1]
Glycyrrhiza Glabra, Kali Muriaticum, Kali Phosphoricum, Iodium, Zincum Gluconicum, Phosphorus, Ascorbicum Acidum, Calcium Gluconate, L-arginine, L-carnitine, L-ornithine, Magnesia Muriatica, Magnesium Gluconicum Dihydricum, Manganese Gluconate, Natrum Muriaticum, Cobalt Gluconate, Copper Gluconate, Creatine, L-glutamine, L-leucine, L-valine, Potassium Gluconate, Selenium Dioxide, Adrenalinum, Boron, Calcarea Phosphorica, Ferrum Sulphuricum, Molybdenum, Niccolum Metallicum, Selenium Metallicum,
Substance Name: [2]
Arginine; Ascorbic Acid; Boron; Calcium Gluconate; Chromium; Cobaltous Gluconate; Copper Gluconate; Corticotropin; Creatine; Dibasic Potassium Phosphate; Epinephrine; Ferrous Sulfate; Glutamine; Glycyrrhiza Glabra; Iodine; Leucine; Levocarnitine; 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]
Labeler Code:
44911
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
01-28-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
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Product Details

What is NDC 44911-0734?

The NDC code 44911-0734 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, kali phosphoricum, iodium, zincum gluconicum, phosphorus, ascorbicum acidum, calcium gluconate, l-arginine, l-carnitine, l-ornithine, magnesia muriatica, magnesium gluconicum dihydricum, manganese gluconate, natrum muriaticum, cobalt gluconate, copper gluconate, creatine, l-glutamine, l-leucine, l-valine, potassium gluconate, selenium dioxide, adrenalinum, boron, calcarea phosphorica, ferrum sulphuricum, molybdenum, niccolum metallicum, selenium 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 44911-0734-1 120 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?

Adults and children take four droppers full twice a day for stamina building and muscle recovery; best if taken 1/2 hour prior to workout. For more strenuous workouts, dosage may be increased to eight droppers full.Consult a physician for use in children under 12 years of age.

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.
  • 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 cm2/mL
  • COPPER GLUCONATE 8 [hp_X]/mL - Derivatives of gluconic acid (the structural formula HOCH2(CHOH)4COOH), including its salts and esters.
  • CORTICOTROPIN 15 [hp_C]/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 12 [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 SULFATE 12 [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.
  • LEVOCARNITINE 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.
  • 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 12 [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.

[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, 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".