Daytime And Nighttime Sinus Relief
NDC Package 0363-9014-24

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 And Nighttime Sinus Relief is ■ take only as directed - see Overdose warning■ do not exceed 4 doses per 24 hours  adults & children 12 years & over 2 softgels with water every 4 hours  children 4 to under 12 years ask a doctor children under 4 years do not use■ when using other Nighttime or Daytime products, carefully readeach label to ensure correct dosing ■ take only as directed - see Overdose warning■ do not exceed 4 doses per 24 hours  adults & children 12 years & over 2 softgels with water every 4 hours  children 4 to under 12 years ask a doctor children under 4 years do not use. Marketed by Walgreens, this product is identified by NDC 0363-9014 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
0363-9014-24
Package Description
1 KIT in 1 PACKAGE, COMBINATION * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
0363-9014
11-Digit Billing Format
00363901424
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 And Nighttime Sinus Relief
Dosage Form
-
Usage Information
■ take only as directed - see Overdose warning■ do not exceed 4 doses per 24 hours  adults & children 12 years & over 2 softgels with water every 4 hours  children 4 to under 12 years ask a doctor children under 4 years do not use■ when using other Nighttime or Daytime products, carefully readeach label to ensure correct dosing ■ take only as directed - see Overdose warning■ do not exceed 4 doses per 24 hours  adults & children 12 years & over 2 softgels with water every 4 hours  children 4 to under 12 years ask a doctor children under 4 years do not use

Regulatory & Marketing

Labeler Name
Walgreens
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-24-2021
Listing Expiration
12-31-2022
Exclude Flag
I
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 0363-9014-24 identifies a specific commercial package of 1 kit in 1 package, combination * 8 capsule, liquid filled in 1 blister pack * 8 capsule, liquid filled in 1 blister pack of Daytime And Nighttime Sinus Relief, labeled by Walgreens. 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 Walgreens on August 24, 2021. The current certification is valid through December 31, 2022.

How is this Walgreens product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363901424. 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)
0363-9014-24
11-Digit CMS (5-4-2)
00363-9014-24

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