Apap Tablet
Product Images NDC 17714-013

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Apap (NDC 17714-013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advance Pharmaceutical Inc., 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

De70766a-figure-01 (De70766a Figure 01)

Packaging label for APAP Extra Strength tablets, containing 500 mg of acetaminophen per tablet. The label identifies it as a pain reliever and fever reducer, with a quantity of 100 tablets per bottle. The labeler is Advance Pharmaceutical Inc., Holtsville, NY. The label also includes drug facts detailing active ingredient, uses, liver warnings, tamper-evident information, and a barcode with NDC 17714-01301.*

FDA Label Image

De70766a-figure-02 (De70766a Figure 02)

Drug Facts panel continuation for APAP (acetaminophen) tablets 500 mg by Advance Pharmaceutical Inc. It includes warnings about use with other acetaminophen drugs, liver disease, and blood thinners, overdose warnings, directions for adults and children 12 years and over, and instructions to ask a doctor for children under 12. It also lists storage conditions, inactive ingredients, and a contact phone number for questions.*

FDA Label Image

De70766a-figure-03 (De70766a Figure 03)

APAP Extra Strength Acetaminophen USP 500 mg oral tablets by Advance Pharmaceutical Inc. The label indicates each tablet contains 500 mg acetaminophen, with a package size of 1000 tablets. The label includes drug facts with uses, warnings, directions, inactive ingredients, and company contact information. The product NDC 17714-013 is stated along with tamper-evident safety instructions.*

* 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.