Daytime Nighttime Intense Flu Relief Kit
NDC Package 0363-3027-02

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

Package Information

Daytime Nighttime Intense Flu Relief (acetaminophen, dextromethorphan hydrobromide, doxylamine succinate) kits is •take only as directed – see Overdose warning•only use the dose cup provided•do not exceed 3 doses (30 mL each) per 24 hrsadults & children 12 yrs & over30 mL every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use •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 kit delivery system. Marketed by Walgreen Company, this product is identified by NDC 0363-3027 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
0363-3027-02
Package Description
1 KIT in 1 CARTON * 355 mL in 1 BOTTLE (0363-4271-40) * 355 mL in 1 BOTTLE (0363-5015-40)
Product Code
0363-3027
11-Digit Billing Format
00363302702

Clinical Specifications

Proprietary Name
Daytime Nighttime Intense Flu Relief
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Dosage Form
Kit - A packaged collection of related material.
Usage Information
•take only as directed – see Overdose warning•only use the dose cup provided•do not exceed 3 doses (30 mL each) per 24 hrsadults & children 12 yrs & over30 mL every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use •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
Walgreen Company
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-10-2026
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 0363-3027-02 identifies a specific commercial package of 1 kit in 1 carton * 355 ml in 1 bottle (0363-4271-40) * 355 ml in 1 bottle (0363-5015-40) of Daytime Nighttime Intense Flu Relief, a human over the counter drug labeled by Walgreen 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 Walgreen Company on July 10, 2026. The current certification is valid through December 31, 2027.

How is this Walgreen Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363302702. 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 (4-4-2)
0363-3027-02
11-Digit CMS (5-4-2)
00363-3027-02

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