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  5. NDC Package Code: 44911-0451-1 Recovatone

NDC Package 44911-0451-1 Recovatone

Glycyrrhiza Glabra,Kali Muriaticum,Zincum Gluconicum,Kali - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
44911-0451-1
Package Description:
120 mL in 1 BOTTLE, DROPPER
Product Code:
44911-0451
Proprietary Name:
Recovatone
Non-Proprietary Name:
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:
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
Usage Information:
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.
11-Digit NDC Billing Format:
44911045101
Product Type:
Human Otc Drug
Labeler Name:
Energique, 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.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ARGININE 6 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • BORON 12 [hp_X]/mL
  • CALCIUM GLUCONATE 6 [hp_X]/mL
  • CARNITINE 6 [hp_X]/mL
  • CHROMIUM 14 [hp_X]/mL
  • COBALTOUS GLUCONATE 8 [hp_X]/mL
  • COPPER GLUCONATE 8 [hp_X]/mL
  • CORTICOTROPIN 6 [hp_X]/mL
  • CREATINE 8 [hp_X]/mL
  • DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL
  • EPINEPHRINE 8 [hp_X]/mL
  • FERROUS GLUCONATE 10 [hp_X]/mL
  • GLUTAMINE 8 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 1 [hp_X]/mL
  • IODINE 4 [hp_X]/mL
  • LEUCINE 8 [hp_X]/mL
  • MAGNESIUM CHLORIDE 6 [hp_X]/mL
  • MAGNESIUM GLUCONATE 6 [hp_X]/mL
  • MANGANESE GLUCONATE 6 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • ORNITHINE 6 [hp_X]/mL
  • PHOSPHORUS 5 [hp_X]/mL
  • POTASSIUM CHLORIDE 2 [hp_X]/mL
  • POTASSIUM GLUCONATE 8 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • SELENIUM DIOXIDE 8 [hp_X]/mL
  • SODIUM CHLORIDE 6 [hp_X]/mL
  • STRONTIUM CARBONATE 12 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
  • VALINE 8 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL
  • ZINC GLUCONATE 4 [hp_X]/mL
    • Pharmacologic Class(es):
  • Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
  • Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
  • Adrenocorticotropic Hormone - [CS]
  • Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
  • Allergens - [CS]
  • Amino Acid - [EPC] (Established Pharmacologic Class)
  • Amino Acids - [CS]
  • Ascorbic Acid - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Catecholamine - [EPC] (Established Pharmacologic Class)
  • Catecholamines - [CS]
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
  • alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
  • beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    04-02-2018
    End Marketing Date:
    09-17-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 44911-0451-1?

    The NDC Packaged Code 44911-0451-1 is assigned to a package of 120 ml in 1 bottle, dropper of Recovatone, a human over the counter drug labeled by Energique, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 44911-0451 included in the NDC Directory?

    Yes, Recovatone with product code 44911-0451 is active and included in the NDC Directory. The product was first marketed by Energique, Inc. on April 02, 2018.

    What is the 11-digit format for NDC 44911-0451-1?

    The 11-digit format is 44911045101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-144911-0451-15-4-244911-0451-01