Day Time Intense Flu Solution
NDC Package 79481-0110-0

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

Package Information

Day Time Intense Flu (acetaminophen, dextromethorphan hydrobromide) solution is •take only as directed – see Overdose warning•only use the dose cup provided•do not exceed 3 doses (30 mL each) per day (24 hrs)adults & children 12 yrs & over30 mL every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use. This formulation utilizes a solution delivery system. Marketed by Meijer, Inc., this product is identified by NDC 79481-0110 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
79481-0110-0
Package Description
355 mL in 1 BOTTLE
Product Code
79481-0110
11-Digit Billing Format
79481011000

Clinical Specifications

Proprietary Name
Day Time Intense Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
•take only as directed – see Overdose warning•only use the dose cup provided•do not exceed 3 doses (30 mL each) per day (24 hrs)adults & children 12 yrs & over30 mL every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use

Regulatory & Marketing

Labeler Name
Meijer, Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-18-2026
Listing Expiration
12-31-2027
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 79481-0110-0 identifies a specific commercial package of 355 ml in 1 bottle of Day Time Intense Flu, a human over the counter drug labeled by Meijer, Inc.. This solution is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide 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 May 18, 2026. The current certification is valid through December 31, 2027.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481011000. 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)
79481-0110-0
11-Digit CMS (5-4-2)
79481-0110-00

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