Acetaminophen Tablet, Film Coated, Extended Release
Product Images NDC 72476-186

2 FDA label images from Retail Business Services,llc. · 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 (NDC 72476-186). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Retail Business Services,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

50 Count (300000552 R 00 Final)

50 Count (300000552 R 00 Final)
Acetaminophen 650 mg extended-release tablets packaging label by Retail Business Services, LLC under the CareOne brand. The label highlights '8 Hour Pain Relief' for minor muscle aches and pain, fever reducer use. It indicates the package contains 50 caplets with a visual of the tablet shape and size. Includes a barcode, product warnings, Drug Facts, and manufacturer details on a predominantly blue background with red and white text elements.*
FDA Label Image

100 Count (300000554 R 00 Final)

100 Count (300000554 R 00 Final)
CareOne 8 Hour Pain Relief Acetaminophen Extended-release Tablets USP, 650 mg oral tablets packaging label. The label states the product is a pain reliever and fever reducer providing up to 8 hours relief of minor muscle aches and pain. It features a blue background with red and white text, includes the quantity of 100 caplets, and shows an image of the actual tablet size. The labeler is Retail Business Services, LLC, and the NDC is 72476-186-10. The packaging advises not to use with other medicines containing acetaminophen.*

* 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.