Acetaminophen Solution
Product Images NDC 0121-1971

3 FDA label images from Pai Holdings, Llc Dba Pai Pharma · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 0121-1971). 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

20 mL Unit Dose Cup Label (Acetaminophen 01)

20 mL Unit Dose Cup Label (Acetaminophen 01)
Label for Acetaminophen oral solution USP, 160 mg/5 mL strength. The label indicates the product is alcohol-free and intended for institutional use only. It includes the National Drug Code (NDC) 02121-657-05, a barcode, and the manufacturer name, Pharmaceutical Associates, Inc., Greenville, SC.*
FDA Label Image

10 mL Unit Dose Cup Label (Acetaminophen 02)

10 mL Unit Dose Cup Label (Acetaminophen 02)
Acetaminophen oral solution USP label displaying 325 mg per 10.15 mL strength. The label indicates alcohol-free formulation intended for institutional use only, packaged by Pharmaceutical Associates, Inc. It includes a barcode and a note to see the insert for details.*
FDA Label Image

5 mL Unit Dose Cup Label (Acetaminophen 03)

5 mL Unit Dose Cup Label (Acetaminophen 03)
Label of Acetaminophen Oral Solution USP, 650 mg per 20.3 mL strength. The label states the product is alcohol-free and for institutional use only. It includes manufacturer details for Pharmaceutical Associates, Inc., Greenville, SC, and a barcode with the NDC 01221-9721-21.*

* 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.