NDC Package 0363-0723-24 Daytime Nighttime Sinus Relief Maximum Strength

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0363-0723-24
Package Description:
1 KIT in 1 CARTON * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Daytime Nighttime Sinus Relief Maximum Strength
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 dosingĀ 
11-Digit NDC Billing Format:
00363072324
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Labeler Name:
Walgreens
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-31-2016
End Marketing Date:
02-28-2025
Listing Expiration Date:
02-28-2025
Exclude Flag:
D
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 0363-0723-24?

The NDC Packaged Code 0363-0723-24 is assigned to a package of 1 kit in 1 carton * 8 blister pack in 1 carton / 1 capsule in 1 blister pack * 16 blister pack in 1 carton / 1 capsule in 1 blister pack of Daytime Nighttime Sinus Relief Maximum Strength, labeled by Walgreens. The product's dosage form is and is administered via form.

Is NDC 0363-0723 included in the NDC Directory?

No, Daytime Nighttime Sinus Relief Maximum Strength with product code 0363-0723 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Walgreens on May 31, 2016 and its listing in the NDC Directory is set to expire on February 28, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0363-0723-24?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

What is the 11-digit format for NDC 0363-0723-24?

The 11-digit format is 00363072324. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20363-0723-245-4-200363-0723-24