Day Cold And Flu And Night Severe Cold And Flu Kit
NDC Package 11673-343-64

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Day Cold And Flu And Night Severe Cold And Flu (acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, dextromethorphan hbr, phenylephrine hcl, triprolidine hcl) kits is usesDay Cold & Flutemporarily relieves these common cold and flu symptoms:coughnasal congestionminor aches and painssore throatheadachestuffy nosesinus congestion and pressuretemporarily reduces fever helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive Night Severe Cold & Flutemporarily relieves these common cold and flu symptoms:coughnasal congestionminor aches and painssore throatheadachesneezingsinus congestion and pressurerunny noseitching of the nose or throatitchy, watery eyes due to hay fevertemporarily reduces fever controls cough to help you get to sleep. This formulation utilizes a kit delivery system. Marketed by Target Corporation, this product is identified by NDC 11673-343 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
11673-343-64
Package Description
4 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK * 6 TABLET, COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
Product Code
11673-343
11-Digit Billing Format
11673034364
RxNorm Crosswalk
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 2549037 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG / triprolidine HCl 1.25 MG Oral Tablet
  • RxCUI: 2549037 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG / triprolidine hydrochloride 1.25 MG Oral Tablet

Clinical Specifications

Proprietary Name
Day Cold And Flu And Night Severe Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl, Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Triprolidine Hcl
Dosage Form
Kit - A packaged collection of related material.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
UsesDay Cold & Flutemporarily relieves these common cold and flu symptoms:coughnasal congestionminor aches and painssore throatheadachestuffy nosesinus congestion and pressuretemporarily reduces fever helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive Night Severe Cold & Flutemporarily relieves these common cold and flu symptoms:coughnasal congestionminor aches and painssore throatheadachesneezingsinus congestion and pressurerunny noseitching of the nose or throatitchy, watery eyes due to hay fevertemporarily reduces fever controls cough to help you get to sleep

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2024
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 11673-343-64 identifies a specific commercial package of 4 blister pack in 1 carton / 1 kit in 1 blister pack * 6 tablet, coated in 1 blister pack * 4 tablet, coated in 1 blister pack of Day Cold And Flu And Night Severe Cold And Flu, a human over the counter drug labeled by Target Corporation. This kit is formulated for oral use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Target Corporation on May 01, 2024. The current certification is valid through December 31, 2026.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673034364. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
11673-343-64
11-Digit CMS (5-4-2)
11673-0343-64

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.