Mucinex Tablet, Extended Release
Product Images NDC 68084-572

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mucinex (NDC 68084-572). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

600 mg Mucinex Tablet Blister

600 mg Mucinex Tablet Blister
Mucinex 600 mg tablets extended-release bi-layer label showing the active ingredient guaifenesin. The label includes the American Health Packaging name and location, product NDC 68084-572, and placeholders for lot number and expiration date. Multiple identical labels are shown in a sheet format.*
FDA Label Image

826d39d8 99f6 2582 E053 2991aa0af2d4

826d39d8 99f6 2582 E053 2991aa0af2d4
Mucinex 600 mg extended-release oral tablets in two colors: one blue tablet embossed with "MUCINEX" and one white tablet embossed with "600." Both tablets are oval in shape, shown next to a millimeter scale for size reference.*
FDA Label Image

600 mg Mucinex Carton (Image 01)

600 mg Mucinex Carton (Image 01)
Mucinex 600 mg guaifenesin extended-release bi-layer tablets packaging label by American Health Packaging. The label highlights 12-hour expectorant action, features a diagram of the bi-layer tablet with immediate and extended-release layers, and indicates the package contains 100 tablets (10 x 10). Includes drug facts, warnings, directions, and storage instructions on the label.*

* 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.