Diclofenac Sodium Solution
Product Images NDC 71205-579

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 71205-579). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Chemical Structure (Diclofenac 01)

Chemical structure of Diclofenac Sodium showing the arrangement of chlorine atoms, benzene rings, and a carboxyl group with sodium.*

FDA Label Image

Figure A (Diclofenac 02)

An instructional illustration showing a hand pouring a topical solution from a bottle onto the palm of the other hand. The image depicts the application process of a solution product.*

FDA Label Image

Figure A (Diclofenac 03)

Illustration showing a hand applying Diclofenac Sodium topical solution to a bent knee, demonstrating the proper use of the product on the affected area. The image depicts correct topical application technique.*

FDA Label Image

Figure B (Diclofenac 04)

An instructional line drawing showing a hand applying topical solution onto the knee area, with arrows indicating the direction of application over the skin.*

FDA Label Image

Figure C (Diclofenac 05)

An instructional line drawing depicting application of a topical solution to the bent knee area. The illustration shows a hand dispensing or applying a liquid onto the skin of the knee, demonstrating proper topical use of the medication.*

FDA Label Image

71205-579-15 (Diclofenac 06)

Label for Diclofenac Sodium 1.5% w/w topical solution, 5 fl oz (150 mL), manufactured by Taro Pharmaceuticals Inc. The label indicates each mL contains 16.05 mg of diclofenac sodium. It includes usage instructions stating the product is for external use only and that a medication guide should be dispensed with each package. The labeler is Proficient Rx LP with NDC 71205-579.*

* 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.