Acetaminophen
Product Images NDC 81033-002

3 FDA label images from Kesin Pharma Corporation · 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 81033-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma Corporation, 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

10.15ml Container Label (Apap 10.15ml Label)

10.15ml Container Label (Apap 10.15ml Label)
Label for Acetaminophen oral solution, 160 mg per 5 mL, packaged in a 10 fl oz bottle by Kesin Pharma Corporation. The label displays storage instructions, lot and expiration dates, and indicates the product is free of alcohol, dye, and sugar.*
FDA Label Image

20.3ml Container Label (Apap 20.3ml Label)

20.3ml Container Label (Apap 20.3ml Label)
Label for Acetaminophen oral solution, 160 mg per 5 mL, in a 20.3 mL package from Kesin Pharma Corporation. The label states that each 20.3 mL delivers 650 mg of acetaminophen. Additional information includes storage instructions to store at 68°-77°F, package by Kesin Pharma in Phoenix, AZ, and that the product is alcohol, dye, and sugar free. The label includes the product NDC 81033-002-20 and a lot number area with a blank space.*
FDA Label Image

5ml Container Label (Apap 5ml Label)

5ml Container Label (Apap 5ml Label)
Label for Acetaminophen oral solution by Kesin Pharma Corporation, NDC 81033-002-05. Each 5 mL contains 160 mg of acetaminophen. Instructions note storage at 68 to 77 degrees Fahrenheit. The label includes lot and expiration date fields, a QR code, and indicates the product contains alcohol, dye, and sugar.*

* 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.