Skelaxin
Product Images NDC 21695-123

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 Skelaxin (NDC 21695-123). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Chemical Structure (Cb47d76e A7e3 4bac 8074 8d7e95c6a6eb 01)

Chemical Structure (Cb47d76e A7e3 4bac 8074 8d7e95c6a6eb 01)
Chemical structure diagram of Skelaxin active ingredient. The image shows the molecular structure including carbon, hydrogen, oxygen, and nitrogen atoms arranged in a specific pattern with labeled groups.*
FDA Label Image

Figure 1 (Cb47d76e A7e3 4bac 8074 8d7e95c6a6eb 02)

Figure 1 (Cb47d76e A7e3 4bac 8074 8d7e95c6a6eb 02)
A line graph depicting mean concentrations (ng/mL) of Metaxalone following an 800 mg dose under fasted and fed conditions over 12 hours. Concentration is plotted on the vertical axis and time in hours on the horizontal axis, showing higher concentrations with food intake compared to fasting.*
FDA Label Image

Skelaxin 800mg (Cb47d76e A7e3 4bac 8074 8d7e95c6a6eb 03)

Skelaxin 800mg (Cb47d76e A7e3 4bac 8074 8d7e95c6a6eb 03)
Skelaxin 800 mg tablets label showing the active ingredient metaxalone. The label indicates 100 tablets in the package, marked as RX only. It is manufactured by Corepharma LLC and distributed and packaged by Rebel Distributors Corp. The label includes dosage directions, storage instructions to keep at controlled room temperature between 15°C and 30°C, and a barcode.*

* 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.