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  5. NDC Package Code: 70677-0011-1 Daytime Cold And Flu

NDC Package 70677-0011-1 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:
70677-0011-1
Package Description:
24 CARTON in 1 BLISTER PACK / 1 CAPSULE, LIQUID FILLED in 1 CARTON
Product Code:
70677-0011
Proprietary Name:
Daytime Cold And Flu
Usage Information:
This product is used as Pain relieverCough SuppressantNasal decongestant. Pain reliever, cough suppressant and Nasal decongestant
11-Digit NDC Billing Format:
70677001101
NDC to RxNorm Crosswalk:
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
    • Labeler Name:
    Mckesson
    Sample Package:
    No
    Start Marketing Date:
    11-25-2016
    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 70677-0011-1?

    The NDC Packaged Code 70677-0011-1 is assigned to a package of 24 carton in 1 blister pack / 1 capsule, liquid filled in 1 carton of Daytime Cold And Flu, labeled by Mckesson. The product's dosage form is and is administered via form.

    Is NDC 70677-0011 included in the NDC Directory?

    No, Daytime Cold And Flu with product code 70677-0011 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Mckesson on November 25, 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 70677-0011-1?

    The 11-digit format is 70677001101. 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
    5-4-170677-0011-15-4-270677-0011-01