Kroger Mucus Relief Dm Solution
NDC Package 41226-739-06

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Kroger Mucus Relief Dm (dextromethorphan hbr and guaifenesin) solution is ▪do not take more than 6 doses in any 24-hour period▪measure only with dosing cup provided▪do not use dosing cup with other products▪dose as follows or as directed by a doctor▪mL = milliliter▪adults and children 12 years and older: 20 mL every 4 hours▪children under 12 years of age: Do not use. This formulation utilizes a solution delivery system. Marketed by Kroger Company, this product is identified by NDC 41226-739 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
41226-739-06
Package Description
180 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
41226073906
RxNorm Crosswalk
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
  • RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution

Clinical Specifications

Proprietary Name
Kroger Mucus Relief Dm Maximum Strength
Non-Proprietary Name
Dextromethorphan Hbr And Guaifenesin
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
▪do not take more than 6 doses in any 24-hour period▪measure only with dosing cup provided▪do not use dosing cup with other products▪dose as follows or as directed by a doctor▪mL = milliliter▪adults and children 12 years and older: 20 mL every 4 hours▪children under 12 years of age: Do not use

Regulatory & Marketing

Labeler Name
Kroger Company
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-05-2024
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 41226-739-06 identifies a specific commercial package of 180 ml in 1 bottle of Kroger Mucus Relief Dm Maximum Strength, a human over the counter drug labeled by Kroger Company. This solution is formulated for oral use and contains dextromethorphan hydrobromide; 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 Kroger Company on April 05, 2024. The current certification is valid through December 31, 2026.

How is this Kroger Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41226073906. 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)
41226-739-06
11-Digit CMS (5-4-2)
41226-0739-06

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