Naproxen Tablet, Delayed Release
Product Images NDC 11534-211

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 Naproxen (NDC 11534-211). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunrise Pharmaceutical, 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

Chemical Structure (Naproxen 01)

Chemical Structure (Naproxen 01)
Chemical structure of naproxen, showing its molecular formula C14H14O3 and molecular weight 230.26, with a methoxy group and carboxyl functional group indicated in the diagram.*
FDA Label Image

Principal Display Panel (375 mg Tablet Bottle Label)

Principal Display Panel (375 mg Tablet Bottle Label)
Naproxen 375 mg delayed-release tablets label for oral use. The label indicates the product contains 100 tablets and is distributed by Sunrise Pharmaceutical, Inc. Packaging features include child-resistant containers and storage instructions for controlled room temperature (20° to 25°C). The label displays the NDC 11534-211-01 and a barcode.*
FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Principal Display Panel (500 mg Tablet Bottle Label)
Naproxen 500 mg delayed-release tablets, USP, displayed on a pharmacy label. The label indicates 100 tablets and notes the medication guide should be dispensed to patients. Distributed by Sunrise Pharmaceutical, Inc., Rahway, NJ. Storage instructions specify 20° to 25°C in light-resistant containers, with child-resistant packaging. The label includes an NDC number and barcode.*

* 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.