Acetaminophen Extra Strength Tablet
Product Images NDC 37835-507

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen Extra Strength (NDC 37835-507). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bi-mart, 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

Label (Label 100 Count)

The packaging label for Bi-Mart Acetaminophen Extra Strength tablets features a red and white design with branding at the top. It states 100 caplets of 500 mg each, with active ingredient acetaminophen listed as a pain reliever and fever reducer. The label includes drug facts, warnings, and usage instructions in black text on white background panels adjacent to the main branding. The labeler is Bi-Mart and the product NDC is 37835-507.*

FDA Label Image

Label (Label 250 Count)

The label for Acetaminophen Extra Strength tablets by Bi-Mart shows 250 caplets, each containing 500 mg of acetaminophen. It highlights use as a pain reliever, fever reducer, and non-aspirin option. The label includes detailed Drug Facts outlining active ingredients, uses, warnings, directions, and inactive ingredients. The packaging features a prominent red and yellow color scheme with two white caplet images and the Bi-Mart logo.*

FDA Label Image

Label (Label 500 Count)

The image shows a Bi-Mart Value Pack label for Acetaminophen Extra Strength tablets. The label highlights the active ingredient acetaminophen at a strength of 500 mg per caplet. It is labeled as a pain reliever and fever reducer that is non-aspirin. The package contains 500 caplets. The label also includes drug facts, usage instructions, warnings, and the Bi-Mart brand name prominently displayed.*

* 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.