Acetaminophen Extra Strength Tablet
Product Images NDC 58602-745

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 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)
This appears to be a mix of a few things including gibberish characters, random numbers, and a product description. The recognizable parts appear to be from a bottle of Extra Strength Acetaminophen Gelcaps, 500mg each, for pain relief and reducing fever. The brand appears to be D AUROHEALTH and the bottle contains 500 tablets. However, without context or legible text, it is difficult to determine if there is any additional useful information.*
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)
This is a medication label for Extra Strength Acetaminophen Gelcaps, containing 500mg of Acetaminophen. It is a pain reliever and fever reducer that does not contain Aspirin. The label includes a Drug Facts section and states that the medication is Rapid Release Gels. There is no additional information available.*

* 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.