Apap Tablet
Product Images NDC 17714-014

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Apap (NDC 17714-014). 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

70309c76-figure-01 (70309c76 Figure 01)

APAP Extra Strength 500 mg oral tablets by Advance Pharmaceutical Inc. The label states acetaminophen USP 500 mg per caplet, 100 caplets per bottle. It is labeled as a pain reliever and fever reducer with drug facts, uses, and liver warnings included on the yellow and red label. The label also indicates tamper evidence and manufacturer details in Holtsville, NY.*

FDA Label Image

70309c76-figure-02 (70309c76 Figure 02)

Drug Facts panel for APAP (Acetaminophen) tablets, providing detailed warnings, directions for use by adults and children, storage instructions, inactive ingredients list, and contact information for questions or comments. Includes overdose warning and advisories for specific health conditions and populations.*

FDA Label Image

70309c76-figure-03 (70309c76 Figure 03)

APAP Extra Strength Acetaminophen USP 500 mg oral tablets, packaged as 1000 caplets in a yellow and red box. Label states it is a pain reliever/fever reducer from Advance Pharmaceutical Inc. The label includes a detailed Drug Facts panel with active ingredient information, usage warnings, directions, and storage instructions. The package warns against use in certain conditions and emphasizes keeping out of reach of children. The labeler information and NDC number 17714-014-10 are shown.*

* 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.