Mucus Relief Tablet, Extended Release
NDC Package 85828-723-02

11-digit billing NDC: 85828072302
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Mucus Relief (guaifenesin) tablets is do not crush, chew, or break extended-release tablettake with a full glass of waterthis product can be administered without regard for the timing of mealsadults and children 12 years of age and over: 1 or 2 extended-release tablets every 12 hours. This formulation utilizes a tablet, extended release delivery system. Marketed by Grocery Outlet, Inc., this product is identified by NDC 85828-723 and is authorized under FDA application ANDA217780.

Identification & Billing

NDC Package Code
85828-723-02
Package Description
1 BLISTER PACK in 1 CARTON / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Code
85828-723
11-Digit Billing Format
85828072302
RxNorm Crosswalk
  • RxCUI: 636522 - guaiFENesin 600 MG 12HR Extended Release Oral Tablet
  • RxCUI: 636522 - 12 HR guaifenesin 600 MG Extended Release Oral Tablet
  • RxCUI: 636522 - guaifenesin 600 MG 12 HR Extended Release Oral Tablet

Clinical Specifications

Proprietary Name
Mucus Relief
Non-Proprietary Name
Guaifenesin
Substance Name
Guaifenesin
Dosage Form
Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
GUAIFENESIN 600 mg/1
Pharmacologic Class
Usage Information
Do not crush, chew, or break extended-release tablettake with a full glass of waterthis product can be administered without regard for the timing of mealsadults and children 12 years of age and over: 1 or 2 extended-release tablets every 12 hours. Do not exceed 4 extended-release tablets in 24 hours.children under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Grocery Outlet, Inc.
Product Type
Human Otc Drug
FDA Application #
ANDA217780
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-13-2026
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 85828-723-02 identifies a specific commercial package of 1 blister pack in 1 carton / 20 tablet, extended release in 1 blister pack of Mucus Relief, a human over the counter drug labeled by Grocery Outlet, Inc.. This tablet, extended release is formulated for oral use and contains guaifenesin 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 Grocery Outlet, Inc. on March 13, 2026. The current certification is valid through December 31, 2027.

How is this Grocery Outlet, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85828072302. 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 (5-3-2)
85828-723-02
11-Digit CMS (5-4-2)
85828-0723-02

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