1. Home
  2. Labeler Index
  3. Proficient Rx Lp
  4. 71205-349
  5. NDC Package Code: 71205-349-18 Cold-eeze

NDC Package 71205-349-18 Cold-eeze

Zinc Gluconate Lozenge 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:
71205-349-18
Package Description:
1 BAG in 1 BOX / 18 LOZENGE in 1 BAG
Product Code:
71205-349
Proprietary Name:
Cold-eeze
Non-Proprietary Name:
Zinc Gluconate
Substance Name:
Zinc Gluconate
Usage Information:
Adults and children 12 years and over:•take Cold-EEZE® when you have cold symptoms •completely dissolve a Cold-EEZE® lozenge in mouth (do not chew)•repeat every 2 - 4 hours as needed until all symptoms subside•recommended daily dosage is 6 lozenges for adults and 4 lozenges for ages 12 - 17Children under 12 years of age should consult a healthcare practitioner prior to use
11-Digit NDC Billing Format:
71205034918
Product Type:
Human Otc Drug
Labeler Name:
Proficient Rx Lp
Dosage Form:
Lozenge - A solid preparation containing one or more medicaments, usually in a flavored, sweetened base which is intended to dissolve or disintegrate slowly in the mouth. A lollipop is a lozenge on a stick.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ZINC GLUCONATE 2 [hp_X]/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:
    05-07-2018
    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 71205-349-18?

    The NDC Packaged Code 71205-349-18 is assigned to a package of 1 bag in 1 box / 18 lozenge in 1 bag of Cold-eeze, a human over the counter drug labeled by Proficient Rx Lp. The product's dosage form is lozenge and is administered via oral form.

    Is NDC 71205-349 included in the NDC Directory?

    Yes, Cold-eeze with product code 71205-349 is active and included in the NDC Directory. The product was first marketed by Proficient Rx Lp on May 07, 2018 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 71205-349-18?

    The 11-digit format is 71205034918. 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
    5-3-271205-349-185-4-271205-0349-18