61941-0101 NDC - COLD-EEZE ()

Drug Information

Product NDC: 61941-0101

Proprietary Name: Cold-EEZE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ProPhase Labs, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2005

Package Information

No. Package Code Package Description Billing Unit
161941-0101-124 PACKAGE in 1 CASE (61941-0101-1) / 18 LOZENGE in 1 PACKAGE (61941-0101-8)
261941-0101-248 PACKAGE in 1 CASE (61941-0101-2) / 18 LOZENGE in 1 PACKAGE (61941-0101-8)
361941-0101-3144 PACKAGE in 1 CASE (61941-0101-3) / 18 LOZENGE in 1 PACKAGE (61941-0101-8)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61941-0101The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMECold-EEZEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/1/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEProPhase Labs, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023