Acetaminophen And Ibuprofen Tablet
Product Images NDC 51316-131

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 And Ibuprofen (NDC 51316-131). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cvs, 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

144ct (144ct)

144ct (144ct)
Acetaminophen and Ibuprofen Dual Action Pain Reliever tablets carton by CVS Health. The label indicates the strengths as Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg, with 144 coated caplets per package. The front panel features a heart graphic and highlights that the product contains two medicines, acetaminophen and ibuprofen, for pain relief.*
FDA Label Image

36ct (36)

36ct (36)
Packaging label for CVS Health Dual Action Pain Reliever tablets containing Acetaminophen 250 mg and Ibuprofen (an NSAID) 125 mg. The label shows a blue and orange design with images of caplets, includes Drug Facts and warnings, and lists the product as an oral tablet with a package count of 36 caplets. Manufacturer details and barcode are also visible.*
FDA Label Image

72ct (72)

72ct (72)
The packaging label for CVS Health dual action pain reliever tablets contains acetaminophen 250 mg and ibuprofen 125 mg. The label shows it is an oral tablet form, packaged with 72 coated caplets per bottle. The label includes drug facts, active and inactive ingredients, warnings, directions, and barcode information. The branding features a dark blue background with yellow and white text and includes the CVS Health logo.*

* 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.