NDC Package 43742-2082-1 Electrolyte Plus

Kali Muriaticum,L-arginine,L-carnitine,L-leucine,L-ornithine,L-valine,Magnesia - View Billable Units, 11-Digit Format, RxNorm

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:
43742-2082-1
Package Description:
120 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Electrolyte Plus
Non-Proprietary Name:
Kali Muriaticum, L-arginine, L-carnitine, L-leucine, L-ornithine, L-valine, Magnesia Muriatica, Ascorbicum Acidum, Borax, Chromium Oxydatum, Ferrum Muriaticum, Kali Carbonicum, Magnesium Gluconicum Dihydricum, Natrum Muriaticum, Zincum Gluconicum, Cuprum Metallicum, Kali Phosphoricum, Niccolum Metallicum, Selenium Metallicum, Vanadium Metallicum, Calcarea Carbonica, Calcarea Phosphorica, Manganum Carbonicum
Substance Name:
Arginine; Ascorbic Acid; Chromic Oxide; Copper; Dibasic Potassium Phosphate; Ferric Chloride Hexahydrate; Leucine; Levocarnitine; Magnesium Chloride; Magnesium Gluconate; Manganese Carbonate; Nickel; Ornithine; Oyster Shell Calcium Carbonate, Crude; Potassium Carbonate; Potassium Chloride; Selenium; Sodium Borate; Sodium Chloride; Tribasic Calcium Phosphate; Valine; Vanadium; Zinc Gluconate
Usage Information:
1/2 tsp twice a day, best if taken 1/2 hour prior to workout. For more strenuous workouts dosage may be increased up to 1 tsp. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
43742208201
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, 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.
  • Pharmacologic Class(es):
  • Allergens - [CS]
  • Ascorbic Acid - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Carnitine Analog - [EPC] (Established Pharmacologic Class)
  • Carnitine - [CS]
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Iron - [CS]
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Parenteral Iron Replacement - [EPC] (Established Pharmacologic Class)
  • Phosphate Binder - [EPC] (Established Pharmacologic Class)
  • Phosphate Chelating Activity - [MoA] (Mechanism of Action)
  • 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)
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    10-10-2023
    Listing Expiration Date:
    12-31-2024
    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 43742-2082-1?

    The NDC Packaged Code 43742-2082-1 is assigned to a package of 120 ml in 1 bottle, dropper of Electrolyte Plus, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-2082 included in the NDC Directory?

    Yes, Electrolyte Plus with product code 43742-2082 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on October 10, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43742-2082-1?

    The 11-digit format is 43742208201. 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
    5-4-143742-2082-15-4-243742-2082-01