Acetaminophen Tablet, Film Coated, Extended Release
Product Images NDC 11822-5019

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 11822-5019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rite Aid, 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

Ar100ct (Ra 100ct 1)

Ar100ct (Ra 100ct 1)
Packaging label for Acetaminophen 650 mg extended-release film-coated tablets by Rite Aid. The label is primarily red and yellow, highlighting 8-hour arthritis pain relief and containing 100 caplets. It includes drug facts, warnings, usage directions, ingredients, and barcodes consistent with over-the-counter oral tablets for pain relief.*
FDA Label Image

100ct (Ra 100ct)

100ct (Ra 100ct)
Carton packaging label for Acetaminophen 650 mg extended-release film-coated tablets by Rite Aid. The label states it is for 8-hour muscle pain relief and contains 100 caplets. The product is described as a pain reliever and fever reducer, with capsule-shaped bi-layer tablets. The label includes Drug Facts, usage directions, warnings, inactive ingredients, and labeler information with barcode and NDC 11822-5019.*
FDA Label Image

50ct (Ra 50ct)

50ct (Ra 50ct)
Box packaging label for Acetaminophen 650 mg extended release film-coated tablets by Rite Aid. The label indicates 50 tablets per container, designed for 8-hour muscle pain relief. Text on the label includes drug facts, warnings, directions, inactive ingredients, distributor information, and barcodes. The packaging is predominantly red with white text and branding elements.*

* 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.