Meijer Daytime Nighttime Cold And Flu Softgel Kit
NDC Package 79481-0888-8

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

Package Information

Meijer Daytime Nighttime Cold And Flu Softgel (acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride) kits is • take only as directed• do not exceed 8 softgels per 24 hrs adults & children 12 yrs & over 2 softgels with water every 4 hrs  children 4 to under 12 yrs ask a doctor  children under 4 yrs do not use  • take only as directed• do not exceed 8 softgels per 24 hrs adults & children 12 yrs & over 2 softgels with water every 6 hrs  children 4 to under 12 yrs ask a doctor  children under 4 yrs do not use . This formulation utilizes a kit delivery system. Marketed by Meijer, Inc., this product is identified by NDC 79481-0888.

Identification & Billing

NDC Package Code
79481-0888-8
Package Description
1 KIT in 1 CARTON * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
79481-0888
11-Digit Billing Format
79481088808
RxNorm Crosswalk
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule

Clinical Specifications

Proprietary Name
Meijer Daytime Nighttime Cold And Flu Softgel
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride
Dosage Form
Kit - A packaged collection of related material.
Usage Information
• take only as directed• do not exceed 8 softgels per 24 hrs adults & children 12 yrs & over 2 softgels with water every 4 hrs  children 4 to under 12 yrs ask a doctor  children under 4 yrs do not use  • take only as directed• do not exceed 8 softgels per 24 hrs adults & children 12 yrs & over 2 softgels with water every 6 hrs  children 4 to under 12 yrs ask a doctor  children under 4 yrs do not use 

Regulatory & Marketing

Labeler Name
Meijer, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
07-31-2025
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 79481-0888-8 identifies a specific commercial package of 1 kit in 1 carton * 8 capsule, liquid filled in 1 blister pack * 4 capsule, liquid filled in 1 blister pack of Meijer Daytime Nighttime Cold And Flu Softgel, a human over the counter drug labeled by Meijer, Inc.. 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 Meijer, Inc. on July 31, 2025. The current certification is valid through December 31, 2026.

How is this Meijer, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481088808. 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 (5-4-1)
79481-0888-8
11-Digit CMS (5-4-2)
79481-0888-08

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