Acetaminophen Suspension
Product Images NDC 0121-2823

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 0121-2823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Principal Display Panel (5 mL Cup Label)

Label for Acetaminophen Oral Suspension delivering 160 mg per 5 mL in a grape-flavored, dye-free formula. It is marked as free of ibuprofen, alcohol, and aspirin. The label states the package is not child-resistant and is provided by Pharmaceutical Associates, Inc. in Greenville, SC.*

FDA Label Image

Principal Display Panel (5 mL Cup Label)

Acetaminophen Oral Suspension label showing 325 mg per 10.15 mL strength. The label states dye-free, grape flavor, and that the product is free of ibuprofen, alcohol, and aspirin. It notes that the package is not child-resistant and includes the manufacturer, Pharmaceutical Associates, Inc., Greenville, SC.*

FDA Label Image

Principal Display Panel (5 mL Cup Label)

Label for Acetaminophen Oral Suspension 650 mg per 20.3 mL by PAI Holdings, LLC dba PAI Pharma. The grape-flavored, dye-free suspension is ibuprofen, alcohol, and aspirin free. The label notes the product is a pain reliever and fever reducer, with instructions to shake well before use. It also indicates the package is not child-resistant and provides manufacturer information.*

* 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.