NDC Package 61941-0231-8 Cold-eeze Plus Nighttime Multi-symptom Relief

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
61941-0231-8
Package Description:
3 BLISTER PACK in 1 CARTON / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product Code:
Proprietary Name:
Cold-eeze Plus Nighttime Multi-symptom Relief
Usage Information:
Take Cold-EEZE® Plus Nighttime Multi-Symptom Relief Cold & Flu QuickMelts® at night when you have cold or flu symptomsAdults: Dissolve entire tablet in mouth. Do not chew. Do not swallow whole.Take 1 tablet 1 hour before bedtimeDo not eat or drink for 15 minutes after use, otherwise, drink plenty of fluidsRecommended dose is 1 tablet for adultsAllow 6-8 hours for sleep after taking tabletFor individuals under the age of 18, consult a healthcare practitioner before use
11-Digit NDC Billing Format:
61941023108
Labeler Name:
Prophase Labs, Inc.
Sample Package:
No
Start Marketing Date:
08-15-2016
Listing Expiration Date:
12-31-2017
Exclude Flag:
I
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 61941-0231-8?

The NDC Packaged Code 61941-0231-8 is assigned to a package of 3 blister pack in 1 carton / 6 tablet, orally disintegrating in 1 blister pack of Cold-eeze Plus Nighttime Multi-symptom Relief, labeled by Prophase Labs, Inc.. The product's dosage form is and is administered via form.

Is NDC 61941-0231 included in the NDC Directory?

No, Cold-eeze Plus Nighttime Multi-symptom Relief with product code 61941-0231 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Prophase Labs, Inc. on August 15, 2016 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 61941-0231-8?

The 11-digit format is 61941023108. 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
5-4-161941-0231-85-4-261941-0231-08