Cc 100
Diclofenac Sodium Gel
Product Images NDC 21922-044
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 21922-044). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Encube Ethicals, 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.
Cc 150
Cc 20
Cc 50
Dosing
Diclofenac Sodium Topical Gel, 1% is a nonsteroidal anti-inflammatory drug (NSAID) used for relieving arthritis pain. It comes with a dosing card (EDS0/00) and users should read the product User Guide before use. The gel should not be used for immediate pain relief. The upper body dose is 2.25 inches long (2 grams) while the lower body dose is 4.5 inches long (4 grams).*
Tl 100
This is a topical medication called Encube containing Diclofenac Sodium, a nonsteroidal anti-inflammatory drug (NSAID) that helps relieve pain. The net weight of the product is 3.53 ounces (100 grams).*
Tl 150
This is a product label for Diclofenac Sodium Topical, a non-steroidal anti-inflammatory drug used to relieve arthritis pain. The product is sold in a 5.29 oz (150 g) container under the brand name Encube with the National Drug Code 21922-044.25. There is also some unreadable text and symbols on the label.*
Tl 20
Description not available.*
Tl 50
This is a medication called Diclofenac Sodium Topical, which is used as an arthritis pain reliever. The package contains a 1.76 oz (50 g) tube of the medication. The text also includes an NDC code for tracking purposes. However, there seems to be some errors that make the text difficult to understand.*
* 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.
