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  5. NDC Package Code: 11673-844-24 Daytime Nighttime Severe Cold And Flu

NDC Package 11673-844-24 Daytime Nighttime Severe Cold And Flu

Acetaminophen,Dextromethorphan Hbr, Guaifenesin, / Acetaminophen,Dextromethorphan - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
11673-844-24
Package Description:
24 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
11673-844
Proprietary Name:
Daytime Nighttime Severe Cold And Flu
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Guaifenesin, / Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
Usage Information:
Usestemporarily relieves common cold/flu symptoms:cough due to minor throat & bronchial irritation minor aches & pains headache fever sore throat helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive.
11-Digit NDC Billing Format:
11673084424
NDC to RxNorm Crosswalk:
  • RxCUI: 1426334 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1426334 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1426334 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 2377385 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG Oral Capsule
  • RxCUI: 2377385 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG Oral Capsule
Product Type:
Human Otc Drug
Labeler Name:
Target Corp
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-01-2024
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
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 11673-844-24?

The NDC Packaged Code 11673-844-24 is assigned to a package of 24 blister pack in 1 carton / 1 kit in 1 blister pack * 8 capsule, liquid filled in 1 blister pack * 4 capsule, liquid filled in 1 blister pack of Daytime Nighttime Severe Cold And Flu, a human over the counter drug labeled by Target Corp. The product's dosage form is kit and is administered via form.

Is NDC 11673-844 included in the NDC Directory?

Yes, Daytime Nighttime Severe Cold And Flu with product code 11673-844 is active and included in the NDC Directory. The product was first marketed by Target Corp on July 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 11673-844-24?

The 11-digit format is 11673084424. 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
5-3-211673-844-245-4-211673-0844-24