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  5. NDC Package Code: 61941-0300-1 Cold-eeze Daytime Cold And Flu

NDC Package 61941-0300-1 Cold-eeze Daytime Cold And Flu

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
61941-0300-1
Package Description:
260 mL in 1 BOTTLE, UNIT-DOSE
Product Code:
61941-0300
Proprietary Name:
Cold-eeze Daytime Cold And Flu
Usage Information:
Do not take more than directed(see Overdose warning)measure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctormL = milliliterAdults and children 12 years and older: 20 mL orally every 4 hours, not to exceed 6 doses in 24 hours.Children under 12 years of age: Do not use unless directed by a doctor
11-Digit NDC Billing Format:
61941030001
NDC to RxNorm Crosswalk:
  • RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1116572 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1116572 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG per 10 ML Oral Solution
  • RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine hydrochloride 10 MG per 20 ML Oral Solution
  • RxCUI: 1116572 - APAP 32.5 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution
    • Labeler Name:
    Prophase Labs, Inc.
    Sample Package:
    No
    Start Marketing Date:
    01-01-2016
    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 61941-0300-1?

    The NDC Packaged Code 61941-0300-1 is assigned to a package of 260 ml in 1 bottle, unit-dose of Cold-eeze Daytime Cold And Flu, labeled by Prophase Labs, Inc.. The product's dosage form is and is administered via form.

    Is NDC 61941-0300 included in the NDC Directory?

    No, Cold-eeze Daytime Cold And Flu with product code 61941-0300 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 January 01, 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 61941-0300-1?

    The 11-digit format is 61941030001. 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
    5-4-161941-0300-15-4-261941-0300-01