NDC Package 43742-1516-1 Electrolyte Plus

Boron Citrate,Calcium Gluconate,Chromium Picolinate,Cobalt Gluconate,Copper - 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:
43742-1516-1
Package Description:
120 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Electrolyte Plus
Non-Proprietary Name:
Boron Citrate, Calcium Gluconate, Chromium Picolinate, Cobalt Gluconate, Copper Gluconate, Ferrous Muriaticum, Magnesium Gluconicum Dihydricum, Manganese Gluconate, Potassium Gluconate, Selenium Dioxide, Sodium Gluconate, Zincum Gluconicum, Kali Phosphoricum, Niccolum Metallicum, Vanadium Metallicum, Calcarea Phosphorica
Substance Name:
Boron Citrate; Calcium Gluconate; Chromium Picolinate; Cobaltous Gluconate; Copper Gluconate; Dibasic Potassium Phosphate; Ferric Chloride Hexahydrate; Magnesium Gluconate; Manganese Gluconate; Nickel; Potassium Gluconate; Selenium Dioxide; Sodium Gluconate; Tribasic Calcium Phosphate; Vanadium; Zinc Gluconate
Usage Information:
For the temporary relief of symptoms relating to electrolyte imbalance such as dizziness and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms relating to electrolyte imbalance such as dizziness and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742151601
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.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    08-21-2019
    End Marketing Date:
    03-16-2027
    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 43742-1516-1?

    The NDC Packaged Code 43742-1516-1 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 43742-1516 included in the NDC Directory?

    Yes, Electrolyte Plus with product code 43742-1516 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on August 21, 2019.

    What is the 11-digit format for NDC 43742-1516-1?

    The 11-digit format is 43742151601. 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
    5-4-143742-1516-15-4-243742-1516-01