Naproxen Tablet
Product Images NDC 60687-491

4 FDA label images from American Health Packaging · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naproxen (NDC 60687-491). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp49101

Ahp49101
Image shows two oblong, beige tablets of Naproxen 500 mg oral dosage form. One tablet is imprinted with "G 32" on one side and the other side has the imprint "500." These tablets are consistent with the prescription drug manufactured or labeled by American Health Packaging.*
FDA Label Image

Blister

Blister
Multiple identical pharmaceutical labels for Naproxen Tablet USP 500 mg oral tablets by American Health Packaging. Each label includes the drug name, strength, NDC barcode, and space for expiry and lot number information, indicating packaging for individual tablets or blister packs.*
FDA Label Image

Carton

Carton
Naproxen Tablets, USP 500 mg oral tablets packaging label by American Health Packaging. The label shows a package size of 100 tablets (10 x 10) with NDC 60687-491-01. It includes pharmacist instructions to dispense the medication guide and storage information at controlled room temperature. Distributed by American Health Packaging, Columbus, Ohio.*
FDA Label Image

Structure

Structure
Chemical structure diagrams of Naproxen and Naproxen Sodium. The left structure depicts the molecular formula of Naproxen, and the right shows the sodium salt form labeled Naproxen Sodium.*

* 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.