Daytime Nighttime Cold And Flu Kit
NDC Package 69256-467-24
Package Information
Daytime Nighttime Cold And Flu (acetaminophen dextromethorphan hbr phenylephrine hci doxylaminesucinate) kits is dAYTIMEdo not take more than directed (see Overdose warning)do not take more than 4 doses in any 24-hour period measure only with dosing cup provided. This formulation utilizes a kit delivery system. Marketed by Harris Teeter, Llc, this product is identified by NDC 69256-467 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 30 mL Oral Solution
- RxCUI: 1043400 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
- RxCUI: 1043400 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG per 15 ML Oral Solution
- RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG per 30 ML Oral Solution
- RxCUI: 1043400 - APAP 21.7 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69256 - Harris Teeter, Llc
- 69256-467 - Daytime Nighttime Cold And Flu
- 69256-467-24 - 1 KIT in 1 KIT * 355 mL in 1 BOTTLE * 355 mL in 1 BOTTLE
- 69256-467 - Daytime Nighttime 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 69256-467-24 identifies a specific commercial package of 1 kit in 1 kit * 355 ml in 1 bottle * 355 ml in 1 bottle of Daytime Nighttime Cold And Flu, a human over the counter drug labeled by Harris Teeter, Llc. 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 Harris Teeter, Llc on May 28, 2021. The current certification is valid through December 31, 2026.
How is this Harris Teeter, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69256046724. 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.