Ibuprofen Tablet, Film Coated
Product Images NDC 70518-1409

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 70518-1409). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Mm2 (Ibuprofen 800mg 70518 1409 01)

Label for Ibuprofen 800 mg film-coated tablets, quantity 21, labeled by RemedyRepack Inc. The label indicates prescription use only with NDC 70518-1409-01. Manufacturing information lists Ascend Labs, LLC, Montvale, NJ. Directions advise consulting the package insert and storing at 20-25°C with permitted excursions. Repackaged by RemedyRepack Inc., Indiana, PA.*

FDA Label Image

Mm3 (Ibuprofen 800mg 70518 1409 02)

Label for Ibuprofen 800 mg film-coated tablets, packaged in a quantity of 90. The label indicates it is a prescription drug from RemedyRepack Inc., with manufacturing by Ascend Labs, LLC, Montvale, NJ. Storage instructions and a barcode are also visible.*

FDA Label Image

Mm4 (Ibuprofen 800mg 70518 1409 03)

Label for Ibuprofen 800 mg film-coated tablets, containing a quantity of 14. The product is for oral use and labeled Rx only. The label includes the NDC number 70518-1409-03, manufacturer Ascend Labs, LLC, and repackager RemedyRepack Inc. Directions advise to see package insert and store between 20-25°C with permitted excursions to 15-30°C. A barcode and QR code are also present.*

FDA Label Image

Mm5 (Ibuprofen 800mg 70518 1409 04)

Packaging label for Ibuprofen 800 mg film-coated tablets. The label shows a quantity of 30 tablets, with the labeler as RemedyRepack Inc. The label includes Rx-only status, an NDC barcode, and text advising to keep medication out of reach of children. Storage conditions and manufacturer information (Ascend Labs, LLC) are also visible.*

FDA Label Image

Ibuprofen 800mg 70518 1409 05

Label for Ibuprofen 800 mg oral film-coated tablets, containing 10 tablets per package. The label includes the NDC number 70518-1409-05 and notes repackaging by RemedyRepack Inc. It advises to keep medication out of children's reach and to see the package insert for directions. Manufacturer is Ascend Labs, LLC, Montvale, NJ.*

FDA Label Image

Ibuprofen 800mg 70518 1409 06

Ibuprofen 800 mg film-coated tablet label from RemedyRepack Inc. The label shows a quantity of 100 tablets. It includes the drug name, strength, dosage form, NDC number 70518-1409-06, and manufacturer information: Ascend Labs, LLC, Montvale, NJ. Directions note to see the package insert, with storage temperature guidelines and repackager contact details.*

FDA Label Image

Ibuprofen 800mg 70518 1409 07

Label for Ibuprofen 800 mg film-coated tablets, quantity of 100. The label states it is a prescription drug repackaged by RemedyRepack Inc., with the original manufacturer listed as Ascend Labs, LLC, Montvale, NJ. Directions mention consulting the package insert with storage recommendations.*

FDA Label Image

Ibuprofen 800mg 70518 1409 08

Ibuprofen 800 mg tablet, film coated, single unit package label. The label includes barcode, QR code, prescription-only status, NDC 70518-1409-08, and manufacturer information: Ascend Labs, LLC, Montvale, NJ. It is repackaged by RemedyRepack Inc., Indiana, PA. Storage instructions and warnings to keep out of reach of children are also visible.*

FDA Label Image

Ibuprofen 800mg 70518 1409 09

Label for Ibuprofen 800 mg oral film-coated tablets, quantity 20, manufactured by Ascend Labs, LLC and repackaged by RemedyRepack Inc. The label includes prescription designation (RX ONLY), NDC number 70518-1409-09, and storage instructions. It also features barcodes and a QR code on a white background with purple branding.*

FDA Label Image

Remedy_label (Remedy Label)

Label for Ibuprofen 800 mg film-coated tablets, with a quantity of 30 tablets. The label includes the NDC number 70518-1409-00 and states the product is for prescription use only. It is repackaged by RemedyRepack Inc. and manufactured by Ascend Labs, LLC. Storage instructions and a QR code are also visible.*

FDA Label Image

Ibuprofen-structure (Ibuprofen Structure)

Chemical structure of ibuprofen, showing the molecular arrangement including a benzene ring with isobutyl and carboxylic acid functional groups.*

* 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.