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  5. NDC Package Code: 69256-470-24 Cold And Flu Relief Daytime Non Drowsy

NDC Package 69256-470-24 Cold And Flu Relief Daytime Non Drowsy

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:
69256-470-24
Package Description:
24 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
69256-470
Proprietary Name:
Cold And Flu Relief Daytime Non Drowsy
Usage Information:
Do not take more than directed (see Overdose warning) do not take more than 4 doses in 24 hours adults and children 12 years and over: take 2 softgels with water every 4 hours swallow whole; do not crush, chew, or dissolve children under 12 years: do not use when using other Daytime or Nighttime products, carefully read each label to insure correct dosing
11-Digit NDC Billing Format:
69256047024
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:
    Harris Teeter, Llc
    Sample Package:
    No
    Start Marketing Date:
    02-28-2015
    Listing Expiration Date:
    12-31-2018
    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 69256-470-24?

    The NDC Packaged Code 69256-470-24 is assigned to a package of 24 blister pack in 1 carton / 1 capsule, liquid filled in 1 blister pack of Cold And Flu Relief Daytime Non Drowsy, labeled by Harris Teeter, Llc. The product's dosage form is and is administered via form.

    Is NDC 69256-470 included in the NDC Directory?

    No, Cold And Flu Relief Daytime Non Drowsy with product code 69256-470 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Harris Teeter, Llc on February 28, 2015 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69256-470-24?

    The 11-digit format is 69256047024. 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 5-3-2 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
    5-3-269256-470-245-4-269256-0470-24