Acetaminophen Tablet, Film Coated
Product Images NDC 49483-341

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 49483-341). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Time Cap Labs Inc, 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

341r Acetamoniphen 500mg Tablets Ct500 Bottle Label

The label for ACETAMINOPHEN Extra Strength pain reliever, 500 mg caplets, manufactured by Time Cap Labs Inc. The package shows 500 caplets and highlights its use as a pain reliever and fever reducer for adults. The label includes Drug Facts, warnings, directions, and inactive ingredients in black and yellow text on a red and white background with the "timely" logo at the top left.*

FDA Label Image

341r Timely Acetaminophen 500mg Bottle Label 1000s

The image shows a packaging label for ACETAMINOPHEN Extra Strength 500 mg film-coated tablets, labeled as pain reliever and fever reducer. The package contains 1000 caplets and is distributed by TIME CAP LABS INC. The label includes detailed Drug Facts with active ingredient, uses, warnings, directions, and inactive ingredients information.*

FDA Label Image

341r Timely Acetaminophen 500mg Bottle Label 100s

Packaging label for ACETAMINOPHEN Extra Strength 500 mg film-coated tablets by Time Cap Labs Inc. The label indicates this is an oral human OTC drug with 100 caplets per container. The label highlights its use as a pain reliever and fever reducer. The NDC 49483-341 is visible, along with usage, warnings, and inactive ingredient information on a drug facts panel.*

* 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.