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  5. NDC Package Code: 71179-350-24 Cold-eeze Cold Remedy Ultramelt Chews

NDC Package 71179-350-24 Cold-eeze Cold Remedy Ultramelt Chews

Zinc Gluconate Tablet, Chewable Oral - 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:
71179-350-24
Package Description:
2 BLISTER PACK in 1 BOX / 12 TABLET, CHEWABLE in 1 BLISTER PACK
Product Code:
71179-350
Proprietary Name:
Cold-eeze Cold Remedy Ultramelt Chews
Non-Proprietary Name:
Zinc Gluconate
Substance Name:
Zinc Gluconate
Usage Information:
• take one chewable tablet at the onset of symptoms • chew slowly and dissolve completely in mouth before swallowing • do not swallow whole • do not eat or drink for 15 minutes after use • repeat every 2-4 hours until symptoms subside Adults 18 years and overdo not exceed 6 chewable tablets per dayChildren 12 to under 18 yearsdo not exceed 4 chewable tablets per dayChildren under 12 yearsask a doctor before use
11-Digit NDC Billing Format:
71179035024
Product Type:
Human Otc Drug
Labeler Name:
Vespyr Brands Inc
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ZINC GLUCONATE 13.3 mg/1
    • Pharmacologic Class(es):
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    07-01-2021
    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 71179-350-24?

    The NDC Packaged Code 71179-350-24 is assigned to a package of 2 blister pack in 1 box / 12 tablet, chewable in 1 blister pack of Cold-eeze Cold Remedy Ultramelt Chews, a human over the counter drug labeled by Vespyr Brands Inc. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 71179-350 included in the NDC Directory?

    Yes, Cold-eeze Cold Remedy Ultramelt Chews with product code 71179-350 is active and included in the NDC Directory. The product was first marketed by Vespyr Brands Inc on July 01, 2021 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 71179-350-24?

    The 11-digit format is 71179035024. 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 5-3-2 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
    5-3-271179-350-245-4-271179-0350-24