Daytime Nighttime Kit
NDC Package 41226-678-02
Package Information
Daytime Nighttime (acetaminophen, guaifenesin, acetaminophen, dextromethorphan hbr, triprolidine hcl) kits is daytimetemporarily relieves these common cold and flu symptoms:minor aches and painsheadachesore throathelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily reduces fever Nighttimetemporarily relieves these common cold and flu symptoms:coughminor aches and painssore throatheadacherunny nosesneezingitching 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 Kroger Company, this product is identified by NDC 41226-678 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 2549034 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / triprolidine HCl 1.25 MG Oral Tablet
- RxCUI: 2549034 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet
- RxCUI: 2549034 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet
- RxCUI: 2717656 - {1 (acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet) / 1 (acetaminophen 325 MG / guaifenesin 200 MG Oral Tablet) } Pack
- RxCUI: 2717656 - 1 daytime (acetaminophen 325 MG / guaiFENesin 200 MG Oral Tablet) / 1 nighttime (acetaminophen 325 MG / dextromethorphan HBr 10 MG / triprolidine HCl 1.25 MG Oral Tablet) Pack
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 41226 - Kroger Company
- 41226-678 - Daytime Nighttime
- 41226-678-02 - 2 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
- 41226-678 - Daytime Nighttime
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 41226-678-02 identifies a specific commercial package of 2 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 Daytime Nighttime, a human over the counter drug labeled by Kroger Company. 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 Kroger Company on July 05, 2025. The current certification is valid through December 31, 2026.
How is this Kroger Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 41226067802. 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.
