Leader Mucus Relief Dm Tablet, Extended Release
Product Images NDC 70000-0722

View Photos of 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 Leader Mucus Relief Dm (NDC 70000-0722). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 110, Llc. Dba Leader, 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-relief-dm-carton-image-1 (219c9e9c2 Image 1)

Mucus-relief-dm-carton-image-1 (219c9e9c2 Image 1)
The packaging label for Leader Mucus Relief DM extended-release tablets features a red and green color scheme. It highlights active ingredients guaifenesin 600 mg and dextromethorphan hydrobromide 30 mg. The label states the product is an expectorant and cough suppressant with 20 tablets per container. It includes a comparison to Mucinex DM active ingredients and a 100% money-back guarantee. Cardinal Health 110, LLC is the labeler.*
FDA Label Image

Mucus-relief-dm-carton-image-2 (219c9e9c2 Image 2)

Mucus-relief-dm-carton-image-2 (219c9e9c2 Image 2)
Leader Mucus Relief DM 30 mg/600 mg extended-release tablets packaging label. The label shows a white and red color scheme with the Leader brand logo. The bottle contains 20 tablets and is for oral use. Active ingredients listed are dextromethorphan hydrobromide 30 mg and guaifenesin 600 mg. The label includes Drug Facts, usage instructions, warnings, and contact information. The product is manufactured by Cardinal Health 110, LLC. dba Leader and the NDC is 70000-0722.*

* 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.