Diclofenac Sodium Gel
Product Images NDC 69097-720

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 69097-720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cipla Usa 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.

FDA Label Image

Carton-label-bora (Carton Label Bora)

Diclofenac Sodium Topical Gel, 1% (10 mg/g) in a 100 g (3.53 oz) tube package. It is labeled as an NSAID arthritis pain reliever for topical external use only. The label includes dosing instructions, treatment areas illustration, active ingredients, drug facts, and manufacturer information from Cipla USA Inc. The packaging emphasizes original prescription strength and includes a dosing card instruction.*

FDA Label Image

Dosing-card (Dosing Card)

Dosing card for Diclofenac sodium topical gel 1%, an arthritis pain reliever. The label includes dosing information showing upper body dose as 2.25 inches long (2 grams) and lower body dose as 4.5 inches long (4 grams). It advises to read the user guide before use and notes it is not for immediate pain relief.*

FDA Label Image

Tube-label-dpt (Tube Label Dpt)

Label for Diclofenac Sodium Topical Gel, 1%, a 10 mg/g NSAID arthritis pain reliever gel by Cipla USA Inc. The label indicates a net weight of 100 g (3.53 oz) and includes directions for opening, warnings, and storage instructions. It shows usage precautions and manufacturer information, including the product NDC 69097-720-44.*

* 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.