Acetaminophen Extra Strength Tablet
Product Images NDC 55319-062

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Acetaminophen Extra Strength (NDC 55319-062). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Family Dollar Stores, Llc, 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

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Label) (Acetaminophen Fig1)

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Label) (Acetaminophen Fig1)
The packaging label for Acetaminophen Extra Strength Gelcaps displays the product name with strength 500 mg, in a dosage form of gelcaps. It is marketed by Family Dollar Stores, LLC and contains 50 gelcaps per package. The label highlights that the product serves as a pain reliever and fever reducer with rapid release gels. The NDC number 55319-062-50 appears on the label.*
FDA Label Image

Package Label-principal Display Panel 500 mg (50 Gelcaps Container Carton) (Acetaminophen Fig2)

Package Label-principal Display Panel 500 mg (50 Gelcaps Container Carton) (Acetaminophen Fig2)
Acetaminophen Extra Strength Pain Relief Gelcaps, 500 mg oral tablets, presented in a box label for 50 gelcaps by Family Dollar Stores, LLC. The label highlights rapid release and pain relief/fever reducer use, with an image of a red and blue gelcap. Additional text includes drug facts, warnings, inactive ingredients, storage instructions, and distributor information (Midwood Brands, LLC).*

* 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.