Acetaminophen Extra Strength Tablet
Product Images NDC 58602-745

2 FDA label images from Aurohealth Llc · 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 Extra Strength (NDC 58602-745). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Label) (Acetaminophen Fig1)

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Label) (Acetaminophen Fig1)
Label for Acetaminophen Extra Strength tablets by Aurohealth LLC, containing 500 mg per tablet. The label states 'Acetaminophen Gelcaps 500 mg,' describing the product as a pain reliever and fever reducer in rapid release gelcap form. The package contains 100 gelcaps. Additional drug facts and warnings are presented on the label, indicating the product is for adult use.*
FDA Label Image

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Carton) (Acetaminophen Fig2)

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Carton) (Acetaminophen Fig2)
Packaging label for Acetaminophen Extra Strength Gelcaps 500 mg by Aurohealth LLC. The red and white carton contains 100 rapid release gelcaps. Label highlights it is a pain reliever and fever reducer for adults, with detailed Drug Facts, warnings, directions, and inactive ingredients listed. Distributed by Aurohealth LLC, East Windsor, NJ.*

* 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.