Acetaminophen Tablet
Product Images NDC 11673-167

View Photos of 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 11673-167). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target 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

100ct Label (100ct)

100ct Label (100ct)
Acetaminophen extra strength 500 mg oral gelcaps label by Target Corporation. The label states the product is a rapid release pain reliever and fever reducer, presented in a 100 gelcaps package. The front label shows a red and blue gelcap image and includes drug facts, uses, warnings, and directions for use in fine print on the back side.*
FDA Label Image

225ct Label (225ct)

225ct Label (225ct)
Packaging label for Up & Up Extra Strength Acetaminophen Gelcaps, 500 mg, an oral tablet product by Target Corporation. The label indicates 225 gelcaps in the container, highlighting rapid release and use as a pain reliever and fever reducer for adults. The label includes a Drug Facts panel with dosage and ingredient information, as well as a capsule size image.*
FDA Label Image

50ct Carton (50ct)

50ct Carton (50ct)
Acetaminophen extra strength 500 mg gelcaps packaging label from Target Corporation. The label shows 50 gelcaps with active ingredient acetaminophen USP, 500 mg per cap. Dosage form is oral gelcaps with external branding by Target and detailed Drug Facts, warnings, directions, and ingredient information on the sides. The product is NDC 11673-167 and made in India.*

* 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.