Mucus Relief D Tablet, Multilayer, Extended Release
NDC Package 0363-8708-68

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

Package Information

Mucus Relief D (guaifenesin and pseudoephedrine hydrochloride) tablets is •do not crush, chew, or break tablet•take with a full glass of water•this product can be administered without regard for timing of meals•adults and children 12 years and older: 2 tablets every 12 hours; not more than 4 tablets in 24 hours•children under 12 years of age: do not use. This formulation utilizes a tablet, multilayer, extended release delivery system. Marketed by Walgreen Company, this product is identified by NDC 0363-8708 and is authorized under FDA application ANDA214407.

Identification & Billing

NDC Package Code
0363-8708-68
Package Description
2 BLISTER PACK in 1 CARTON / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
Product Code
0363-8708
11-Digit Billing Format
00363870868
RxNorm Crosswalk
  • RxCUI: 1305603 - guaiFENesin 600 MG / pseudoephedrine HCl 60 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1305603 - 12 HR guaifenesin 600 MG / pseudoephedrine hydrochloride 60 MG Extended Release Oral Tablet
  • RxCUI: 1305603 - guaifenesin 600 MG / pseudoephedrine hydrochloride 60 MG 12 HR Extended Release Oral Tablet

Clinical Specifications

Proprietary Name
Mucus Relief D
Non-Proprietary Name
Guaifenesin And Pseudoephedrine Hydrochloride
Substance Name
Guaifenesin; Pseudoephedrine Hydrochloride
Dosage Form
Tablet, Multilayer, Extended Release - A solid dosage form containing medicinal substances that have been compressed to form a multiple-layered tablet or a tablet-within-a-tablet, the inner tablet being the core and the outer portion being the shell, which, additionally, is covered in a designated coating; the tablet is formulated in such manner as to allow at least a reduction in dosing frequency as compared to that drug presented as a conventional dosage form.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
•do not crush, chew, or break tablet•take with a full glass of water•this product can be administered without regard for timing of meals•adults and children 12 years and older: 2 tablets every 12 hours; not more than 4 tablets in 24 hours•children under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Walgreen Company
Product Type
Human Otc Drug
FDA Application #
ANDA214407
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-26-2024
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 0363-8708-68 identifies a specific commercial package of 2 blister pack in 1 carton / 18 tablet, multilayer, extended release in 1 blister pack of Mucus Relief D, a human over the counter drug labeled by Walgreen Company. This tablet, multilayer, extended release is formulated for oral use and contains guaifenesin; pseudoephedrine hydrochloride 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 March 26, 2024. The current certification is valid through December 31, 2026.

How is this Walgreen Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363870868. 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)
0363-8708-68
11-Digit CMS (5-4-2)
00363-8708-68

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