Daytime Cold And Flu
NDC Package 79481-0026-2

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Daytime Cold And Flu is take only as directed—see Overdose warning. Marketed by Meijer, Inc, this product is identified by NDC 79481-0026 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
79481-0026-2
Package Description
2 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
79481-0026
11-Digit Billing Format
79481002602
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

Clinical Specifications

Proprietary Name
Daytime Cold And Flu
Dosage Form
-
Usage Information
Take only as directed—see Overdose warning. do not exceed 4 doses per 24 hours.adults and children 12 years of age and overswallow 2 softgels with water every 4 hourschildren 4 to under 12 years of ageask a doctorchildren under 4 years of agedo not useWhen using other Daytime or Nighttime products, carefully read each label to insure correct dosing

Regulatory & Marketing

Labeler Name
Meijer, Inc
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-12-2022
Listing Expiration
12-31-2025
Exclude Flag
I
Sample Package
Yes

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 79481-0026-2 identifies a specific commercial package of 2 blister pack in 1 carton / 12 capsule, liquid filled in 1 blister pack of Daytime Cold And Flu, labeled by Meijer, Inc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Meijer, Inc on September 12, 2022. The current certification is valid through December 31, 2025.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481002602. 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)
79481-0026-2
11-Digit CMS (5-4-2)
79481-0026-02

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