Medique Cold Eeze Lozenge
NDC Package 47682-478-73

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Medique Cold Eeze (zinc gluconate) lozenges is take one lozenge at the onset of symptoms dissolve entire lozenge in mouth do not chew do not swallow whole do not eat or drink for 15 minutes after use repeat every 2-4 hours until symptoms subsideAdults and children 18 years and over: do not exceed 6 lozenges per day Children 12 to 18 years: do not exceed 4 lozenges per day Children under 12 years: ask a doctor before use. This formulation utilizes a lozenge delivery system. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-478.

Identification & Billing

NDC Package Code
47682-478-73
Package Description
25 LOZENGE in 1 CARTON
Product Code
11-Digit Billing Format
47682047873

Clinical Specifications

Proprietary Name
Medique Cold Eeze
Non-Proprietary Name
Zinc Gluconate
Substance Name
Zinc Gluconate
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
take one lozenge at the onset of symptoms dissolve entire lozenge in mouth do not chew do not swallow whole do not eat or drink for 15 minutes after use repeat every 2-4 hours until symptoms subsideAdults and children 18 years and over: do not exceed 6 lozenges per day Children 12 to 18 years: do not exceed 4 lozenges per day Children under 12 years: ask a doctor before use

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-07-2020
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 47682-478-73 identifies a specific commercial package of 25 lozenge in 1 carton of Medique Cold Eeze, a human over the counter drug labeled by Unifirst First Aid Corporation. This lozenge is formulated for oral use and contains zinc gluconate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Unifirst First Aid Corporation on April 07, 2020. The current certification is valid through December 31, 2026.

How is this Unifirst First Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 47682047873. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
47682-478-73
11-Digit CMS (5-4-2)
47682-0478-73

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.