Mucus Dm Extended Release Tablet, Extended Release
Product Images NDC 69842-812

2 FDA label images from Cvs Pharmacy · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mucus Dm Extended Release (NDC 69842-812). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cvs Pharmacy, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Mucus Dm Extended Release Carton Image 1 (8126617c1 Image 1)

Mucus Dm Extended Release Carton Image 1 (8126617c1 Image 1)
Packaging label for CVS Health Maximum Strength Mucus DM Extended Release tablets containing guaifenesin and dextromethorphan hydrobromide 1200 mg/60 mg. The label highlights its use as an expectorant and cough suppressant with 14 extended-release tablets per bottle. Includes a depiction of the tablet size and a bottle outline indicating package contents. The product is labeled for 12-hour relief.*
FDA Label Image

Mucus Dm Extended Release Carton Image 2 (8126617c1 Image 2)

Mucus Dm Extended Release Carton Image 2 (8126617c1 Image 2)
Mucus DM Extended Release tablets, maximum strength, containing guaifenesin 1200 mg and dextromethorphan hydrobromide 60 mg. The extended-release oral tablets are labeled as expectorant and cough suppressant. Packaged by CVS Pharmacy, the label features directions, warnings, and other drug facts, highlighting a 12-hour dosing interval and safety information for use.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.