NDC Package 67510-9156-0 Multi Sympton Cold Day Night

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:
67510-9156-0
Package Description:
1 KIT in 1 PACKAGE, COMBINATION * 1 BLISTER PACK in 1 BOX (67510-4156-1) / 10 TABLET in 1 BLISTER PACK * 1 BLISTER PACK in 1 BOX (67510-3156-1) / 10 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Multi Sympton Cold Day Night
Usage Information:
Do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 tablets every 4 hoursswallow whole - do not crush, chew or dissolvedo not take more than 12 tablets in 24 hourschildren under 12 yearsDo not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage
11-Digit NDC Billing Format:
67510915600
NDC to RxNorm Crosswalk:
  • RxCUI: 1086991 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1086991 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1086991 - APAP 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1094538 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1094538 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • Labeler Name:
    Kareway Product, Inc.
    Sample Package:
    No
    Start Marketing Date:
    05-01-2012
    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 67510-9156-0?

    The NDC Packaged Code 67510-9156-0 is assigned to a package of 1 kit in 1 package, combination * 1 blister pack in 1 box (67510-4156-1) / 10 tablet in 1 blister pack * 1 blister pack in 1 box (67510-3156-1) / 10 tablet in 1 blister pack of Multi Sympton Cold Day Night, labeled by Kareway Product, Inc.. The product's dosage form is and is administered via form.

    Is NDC 67510-9156 included in the NDC Directory?

    No, Multi Sympton Cold Day Night with product code 67510-9156 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Kareway Product, Inc. on May 01, 2012 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 67510-9156-0?

    The 11-digit format is 67510915600. 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
    5-4-167510-9156-05-4-267510-9156-00