Diclofenac Sodium Gel
Product Images NDC 68001-621

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 68001-621). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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 Label (Diclofenac Sodium Topical Gel Carton Label)

The unfolded packaging label for Diclofenac Sodium Topical Gel, 1%, a topical NSAID pain reliever by BluePoint Laboratories. The label includes product name, strength (10 mg/g), usage instructions, drug facts, warnings, and a barcode. The package states it is for external use, helps relieve arthritis pain and inflammation, and includes typical OTC drug labeling with directions and precautions.*

FDA Label Image

Container Label (Diclofenac Sodium Topical Gel Tube Label)

Label for Diclofenac Sodium Topical Gel 1%, a 10 mg/g topical NSAID gel by BluePoint Laboratories. The label indicates a net weight of 3.53 oz (100 g) and includes warnings about allergic reactions, liver damage, stomach bleeding, and heart risks. It also states storage instructions and a customer service phone number.*

FDA Label Image

Dosing Card (Dosing Card)

A dosing card for Diclofenac Sodium Topical Gel 1% indicating approximate doses: 2.25 inches long (2 grams) for upper body use and 4.5 inches long (4 grams) for lower body use. It advises reading the product User Guide before use and notes it is not for immediate pain relief.*

* 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.