Daytime Nighttime Sinus Relief Kit
NDC Package 0363-0744-24

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

Package Information

Daytime Nighttime Sinus Relief (acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl/acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl) kits is dAYTIMEdo not take more than directed (see Overdose warning)do not take more than 12 softgels (Daytime and NightTime) in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label to ensure correct dosingNIGHTTIMEdo not take more than directed (see Overdose warning)do not take more than 12 softgels (Daytime and Nighttime) in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label to ensure correct dosing . This formulation utilizes a kit delivery system. Marketed by Walgreens, this product is identified by NDC 0363-0744 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
0363-0744-24
Package Description
3 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK * 4 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK
Product Code
0363-0744
11-Digit Billing Format
00363074424
RxNorm Crosswalk
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1297288 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
Daytime Nighttime Sinus Relief Maximum Strength
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl/acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, Phenylephrine Hcl
Dosage Form
Kit - A packaged collection of related material.
Usage Information
DAYTIMEdo not take more than directed (see Overdose warning)do not take more than 12 softgels (Daytime and NightTime) in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label to ensure correct dosingNIGHTTIMEdo not take more than directed (see Overdose warning)do not take more than 12 softgels (Daytime and Nighttime) in any 24-hour periodadults and children 12 years of age and older: take 2 softgels every 4 hourschildren under 12 years of age: do not usewhen using other Daytime or Nighttime products, carefully read each label to ensure correct dosing 

Regulatory & Marketing

Labeler Name
Walgreens
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2022
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 0363-0744-24 identifies a specific commercial package of 3 blister pack in 1 carton / 1 kit in 1 blister pack * 4 capsule in 1 blister pack * 8 capsule in 1 blister pack of Daytime Nighttime Sinus Relief Maximum Strength, a human over the counter drug labeled by Walgreens. 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 Walgreens on June 01, 2022. The current certification is valid through December 31, 2026.

How is this Walgreens product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363074424. 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)
0363-0744-24
11-Digit CMS (5-4-2)
00363-0744-24

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