Uline Acetaminophen Extra Strength Tablet, Film Coated
Product Images NDC 69790-154

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Uline Acetaminophen Extra Strength (NDC 69790-154). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Uline, 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

Uline Acetaminophen Xs Label 20

Uline Acetaminophen Extra Strength 500 mg packaging label displays the brand name Uline prominently. The label highlights the product as a pain reliever and fever reducer with 50 packets, each containing 2 tablets. It includes tamper-evident sealed packet warnings and usage instructions for households without young children. Drug Facts panel details active ingredient dosage, uses, warnings, directions, and inactive ingredients.*

FDA Label Image

Uline Apap Xs Label 20

Uline Acetaminophen Extra Strength 500 mg packaging label featuring a red and white design. The label states the product is a pain reliever and fever reducer with 50 packets, each containing 2 tablets. The labeler is Uline.*

* 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.