Acetaminophen 500 Mg Tablet
Product Images NDC 72090-038

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 Acetaminophen 500 Mg (NDC 72090-038). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pioneer Life Sciences, Llc, 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

Pl0232-00 Gc Pain Relief Es 500ct_page-0001 (Pl0232 00 Gc Pain Relief Es 500ct Page 0001)

Pl0232-00 Gc Pain Relief Es 500ct_page-0001 (Pl0232 00 Gc Pain Relief Es 500ct Page 0001)
The image shows the packaging label for ACETAMINOPHEN 500 mg extra strength caplets by GenCare, a generic healthcare brand. The label highlights the product as a pain reliever and fever reducer with 500 caplets per package. It includes a Drug Facts panel listing acetaminophen 500 mg as the active ingredient, usage instructions, warnings about liver safety and overdose, and additional inactive ingredients. The package design uses red and yellow colors with an illustration of two white caplets. The labeler is Pioneer Life Sciences, LLC.*
FDA Label Image

Pl0233-00 Gc Pain Relief Es 300ct_page-0001 (Pl0233 00 Gc Pain Relief Es 300ct Page 0001)

Pl0233-00 Gc Pain Relief Es 300ct_page-0001 (Pl0233 00 Gc Pain Relief Es 300ct Page 0001)
The packaging label for ACETAMINOPHEN 500 mg extra strength tablets, a pain reliever and fever reducer by GenCare under Pioneer Life Sciences. The label indicates 300 caplets for adults, with dosage instructions, active ingredients, warnings, and storage information. The label also emphasizes it is a generic version comparable to Tylenol Extra Strength caplets.*

* 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.