Ibuprofen Tablet, Film Coated
Product Images NDC 72189-231

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 72189-231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

231 (72189 0231 21)

IBUPROFEN 600 mg film-coated tablets bottle label by DIRECT RX. The label shows the dosage strength 600 mg with 21 tablets per bottle. It states the product is generic for MOTRIN with each tablet containing 600 mg ibuprofen. Lot number, expiration date, NDC, and packaging details are also displayed on the label.*

FDA Label Image

266 (72189 266 40)

IBUPROFEN 800 mg film-coated tablets in a blister pack containing 40 tablets. The label indicates the product is generic for Motrin and each tablet contains ibuprofen USP 800 mg. The packaging includes NDC numbers and manufacturing details by Direct RX.*

FDA Label Image

Hi (72189 266 30)

Ibuprofen 800 mg film-coated tablets packaging label from Direct Rx. The label shows 30 tablets per container, with the generic name Motrin indicated. Lot and expiration details are printed, along with NDC 72189-266-30. The label highlights each tablet contains 800 mg of ibuprofen.*

FDA Label Image

Hjshdkshfkj (72189 266 90)

Packaging label for IBUPROFEN 800 mg film-coated tablets by DIRECT RX. The label indicates the package contains 90 tablets and states the product is generic for Motrin. The NDC (72189-266-90) is visible along with manufacturing and expiration details.*

FDA Label Image

67836482764 (72189 266 71)

Ibuprofen 800 mg film-coated tablets, 100 count carton label. The package is labeled as generic for Motrin, containing ibuprofen USP 800 mg per tablet. The product is packaged and distributed by Direct Rx. The label includes lot, expiration, and NDC numbers.*

FDA Label Image

Yugthgistueg (72189 266 72)

Label for IBUPROFEN 800 mg film-coated tablets, 120 count, manufactured and distributed by DIRECT RX. The label states it is a generic for Motrin, with each tablet containing 800 mg of ibuprofen USP. Additional labeling information includes lot number 22DE2123, expiration date 5/31/23, and manufacturing site in Dawsonville, GA.*

FDA Label Image

Yugthgistueg (72189 266 60)

IBUPROFEN 800 mg film-coated tablets in a carton label stating 60 tablets per package. The label highlights that the product is a generic for MOTRIN and each tablet contains 800 mg of ibuprofen. The label also includes lot number 22DE2124, expiry date 5/31/23, and is packaged and distributed by DIRECT RX in Dawsonville, Georgia.*

FDA Label Image

72189-231-90 (72189 231 90)

Packaging label for IBUPROFEN 600 mg film-coated tablets, 90 count. The label indicates it is generic for MOTRIN and distributed by DIRECT RX. The label includes the NDC number 72189-231-90 and manufacturing details.*

FDA Label Image

72189-231-60 (72189 231 60)

Packaging label for IBUPROFEN 600 mg film-coated tablets, containing 60 tablets per bottle. The label specifies that the generic equivalent is for MOTRIN. The product is distributed by DIRECT RX and includes batch and expiration details along with NDC numbers.*

FDA Label Image

72189-231-30 (72189 231 30)

Packaging label for IBUPROFEN 600 mg film-coated tablets. The box contains 30 tablets and is identified as a generic version of Motrin. The label includes lot and manufacturing details, showing it is distributed by Direct Rx.*

FDA Label Image

72189-266-15 (72189 266 15)

IBUPROFEN 800 mg film-coated tablets label by DIRECT RX. The yellow and white label indicates a package containing 15 tablets. It specifies ibuprofen, USP 800 mg per tablet, generic for Motrin. The label includes lot number, expiration date (6/30/23), NDC 72189-266-15, and manufacturing location.*

* 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.