Diclofenac Sodium Gel
Product Images NDC 68462-355

View Photos of 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 Diclofenac Sodium (NDC 68462-355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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

Carton (Carton)

Carton (Carton)
This is a description of a medication called Diclofenac Sodium Gel, 3% which is manufactured by Glenmark Pharmaceuticals Ltd. in India. The medication is prescribed for external use only as a topical treatment for actinic keratosis. The standard adult dosage of the medication is 0.5 g (pea size) of gel applied twice a day onto the affected skin. The package insert contains complete dosing information. The medication should be stored at controlled room temperature, between 20° to 25°C (68° to 77°F) and protected from heat and freezing conditions. A crimp of the tube and/or carton indicates the lot number and expiration date. Pharmacists are advised to dispense the enclosed medication guide to each patient.*
FDA Label Image

Structure (Image 01)

FDA Label Image
FDA Label Image

Structure

* 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.