Diclofenac Sodium Solution
Product Images NDC 70512-810

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 70512-810). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sola Pharmaceuticals, Llc, 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 (Carton)

Packaging label for Diclofenac Sodium topical solution USP 1.5% w/w, 5 fl oz (150 mL), by SOLA Pharmaceuticals. The label features dosage instructions, a warning for external use only, and guidance to dispense the enclosed medication guide to each patient. It includes product identification and barcodes, with storage and excipient information in fine print.*

FDA Label Image

Chemical Structure Diagram (Chemicalstructure)

Chemical structure of Diclofenac Sodium showing two chlorine atoms on the aromatic ring, an amide linkage, and a carboxylate group bonded with a sodium ion.*

FDA Label Image

Figure A (Figurea)

An instructional illustration depicting the topical administration of a solution medication. Figure A shows a hand applying the solution to the palm of the opposite hand, while another smaller image shows the application of the solution onto a knee. The images indicate proper external use of the product.*

FDA Label Image

Figure B (Figureb)

An illustration showing a person applying a topical solution to the knee area using fingers, with arrows indicating the motion and direction for application on and around the knee.*

FDA Label Image

Figure C (Figurec)

An illustration labeled Figure C showing a hand applying a topical solution to an arm with a circular arrow, indicating the direction of application.*

FDA Label Image

Label (Label)

Label for Diclofenac Sodium topical solution USP, 1.5% w/w, in a 5 fl oz (150 mL) container. The label states it is manufactured by SOLA Pharmaceuticals, includes directions for use, storage instructions, a warning about skin irritation, and a list of excipients. It emphasizes external use only and provides dosage instructions.*

* 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.