Diclofenac Sodium Gel
Product Images NDC 46708-581

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 Diclofenac Sodium (NDC 46708-581). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Image (Cc529794 6914 479b 8f58 86f5746c2a89 01)

Image (Cc529794 6914 479b 8f58 86f5746c2a89 01)
Chemical structure diagram of diclofenac sodium, showing its molecular arrangement including chlorinated aromatic rings and a carboxylate sodium salt group.*
FDA Label Image

Container Label (Cc529794 6914 479b 8f58 86f5746c2a89 02)

Container Label (Cc529794 6914 479b 8f58 86f5746c2a89 02)
Label for Diclofenac Sodium Topical Gel 3%, a human prescription drug in topical gel form by Alembic Pharmaceuticals Limited. The label includes active ingredient strength (30 mg per gram), NDC 46708-581-31, net weight 100 g, usage instructions, storage conditions, and manufacturer location in Vadodara, India. A barcode is also present.*
FDA Label Image

Carton Label (Cc529794 6914 479b 8f58 86f5746c2a89 03)

Carton Label (Cc529794 6914 479b 8f58 86f5746c2a89 03)
Packaging label for Diclofenac Sodium Topical Gel 3%, a 100 g topical gel product by Alembic Pharmaceuticals Limited. The label includes active ingredient strength (30 mg/g), directions for external use, storage instructions, and batch coding information. The label design features blue and green accents and includes NDC 46708-581-31.*

* 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.