Guaifenesin And Dextromethorphan Hbr Tablet, Extended Release
Product Images NDC 11673-267

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 Guaifenesin And Dextromethorphan Hbr (NDC 11673-267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (1200 mg/60 mg (14 Tablet Bottle))

Package Label-principal Display Panel (1200 mg/60 mg (14 Tablet Bottle))
The image shows packaging labels for Guaifenesin and Dextromethorphan HBr extended-release tablets, 1200 mg/60 mg strength. The front panel highlights "Mucus Relief DM" with a 12-hour effect, sold in a 14-tablet count pack by Target Corporation. Additional panels include Drug Facts with active ingredients, uses, warnings, directions, inactive ingredients, and contact information. The label states the product is made in India.*
FDA Label Image

Package Label-principal Display Panel (1200 mg/60 mg (14 Tablet Carton Label))

Package Label-principal Display Panel (1200 mg/60 mg (14 Tablet Carton Label))
Packaging label for Mucus Relief DM maximum strength extended-release tablets containing 1200 mg Guaifenesin and 60 mg Dextromethorphan HBr. The label shows a 14-tablet bottle with 12-hour cough relief, marketed under the up&up brand by Target Corporation. It highlights active ingredients, directions, warnings, and Drug Facts on a green background with blue and white text.*

* 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.