Maximum Strength Multi-symptom Relief Tablet, Film Coated
NDC Package 41226-674-02
Package Information
Maximum Strength Multi-symptom Relief (acetaminophen, dextromethorphan hbr) tablets is usestemporarily relieves these common cold and flu symptoms:- cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants - the intensity of coughing - the impulse to cough to help you get to sleep- minor aches and pains- sore throat - headache temporarily reduces fever. This formulation utilizes a tablet, film coated delivery system. Marketed by Kroger Company, this product is identified by NDC 41226-674 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 2709673 - acetaminophen 325 MG / dextromethorphan HBr 10 MG Oral Tablet
- RxCUI: 2709673 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG Oral Tablet
- RxCUI: 2709673 - APAP 325 MG / dextromethorphan hydrobromide 10 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 41226 - Kroger Company
- 41226-674 - Maximum Strength Multi-symptom Relief
- 41226-674-02 - 2 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
- 41226-674 - Maximum Strength Multi-symptom Relief
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 41226-674-02 identifies a specific commercial package of 2 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack of Maximum Strength Multi-symptom Relief, a human over the counter drug labeled by Kroger Company. This tablet, film coated is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide 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 June 14, 2025. 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: 41226067402. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.