Daytime Nighttime Severe Cold And Flu Kit
NDC Package 11673-844-24
Package Information
Daytime Nighttime Severe Cold And Flu (acetaminophen, dextromethorphan hbr, guaifenesin, / acetaminophen, dextromethorphan hbr, doxylamine succinate) kits is 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. This formulation utilizes a kit delivery system. Marketed by Target Corp, this product is identified by NDC 11673-844 and is authorized under FDA application M012.
Identification & Billing
- 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
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 11673 - Target Corp
- 11673-844 - Daytime Nighttime Severe Cold And Flu
- 11673-844-24 - 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
- 11673-844 - Daytime Nighttime Severe Cold And Flu
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 11673-844-24 identifies a specific commercial 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. This kit is formulated for 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 Corp on July 01, 2024. The current certification is valid through December 31, 2026.
How is this Target Corp product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673084424. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.