Mucus Relief Tablet, Extended Release
NDC Package 72090-012-01

11-digit billing NDC: 72090001201
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Mucus Relief (guaifenesin) tablets is •do not crush, chew, or break tablet•take with a full glass of water•this product can be administered without regard for the timing of meals•adults and children 12 years of age and over: 1 tablet every 12 hours. This formulation utilizes a tablet, extended release delivery system. Marketed by Pioneer Life Sciences, Llc, this product is identified by NDC 72090-012 and is authorized under FDA application ANDA213420.

Identification & Billing

NDC Package Code
72090-012-01
Package Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code
72090-012
11-Digit Billing Format
72090001201
RxNorm Crosswalk
  • RxCUI: 310621 - guaiFENesin 1200 MG 12HR Extended Release Oral Tablet
  • RxCUI: 310621 - 12 HR guaifenesin 1200 MG Extended Release Oral Tablet
  • RxCUI: 310621 - guaifenesin 1200 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 1200 mg/1
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 the timing of meals•adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours.•children under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Pioneer Life Sciences, Llc
Product Type
Human Otc Drug
FDA Application #
ANDA213420
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-04-2025
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (72090-012). Click a package code to view its specific billing and regulatory data.

72090-012-02
30 TABLET, EXTENDED RELEASE in 1 BOTTLE
72090-012-03
50 TABLET, EXTENDED RELEASE in 1 BOTTLE

* 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 72090-012-01 identifies a specific commercial package of 100 tablet, extended release in 1 bottle of Mucus Relief, a human over the counter drug labeled by Pioneer Life Sciences, Llc. 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 Pioneer Life Sciences, Llc on December 04, 2025. The current certification is valid through December 31, 2026.

How is this Pioneer Life Sciences, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72090001201. 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)
72090-012-01
11-Digit CMS (5-4-2)
72090-0012-01

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