Acetaminophen Extra Strength Tablet
Product Images NDC 21130-155

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 21130-155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Better Living Brands 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)
Acetaminophen Extra Strength 500 mg tablets labeled as Rapid Release Gels by Signature Care. The label indicates 100 gelcaps in the package, each containing 500 mg of acetaminophen. It is an oral pain reliever and fever reducer. The label includes Drug Facts, warnings, and directions for adult use. Distributed by Better Living Brands LLC.*
FDA Label Image

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Carton) (Acetaminophen Fig2)

Package Label-principal Display Panel 500 mg (24 Gelcaps Container Carton) (Acetaminophen Fig2)
Packaging label for Acetaminophen Extra Strength Gelcaps, 500 mg oral tablets distributed by Better Living Brands LLC. The label indicates 100 gelcaps per container with active ingredient Acetaminophen USP 500 mg. It includes usage warnings, drug facts, and storage instructions, along with barcode and manufacturing details. The product is for adults and claims rapid release. The label features a predominantly red design with white text areas for information.*

* 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.