Diclofenac Sodium Solution/ Drops
Product Images NDC 76420-134

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 76420-134). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed 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

Chemical Structure (Diclofenac 01)

Chemical structure of diclofenac sodium, showing a chlorinated biphenyl amine linked to a carboxylate group with a sodium ion counterion.*

FDA Label Image

Figure A (Diclofenac 02)

An instructional diagram showing two methods of applying a liquid solution topically using a dropper. One method depicts drops being applied to the palm of a hand, and the other shows drops applied to the skin of a bent arm.*

FDA Label Image

Figure B (Diclofenac 03)

An instructional illustration showing a hand applying a product to the knee area with downward arrows indicating the direction of application, suggesting how to use a topical solution on the skin around a joint.*

FDA Label Image

Figure C (Diclofenac 04)

An instructional line drawing showing a hand applying a patch or medication to the skin of an arm, with an arrow indicating a circular motion for application. The image depicts a step in the transdermal administration process.*

FDA Label Image

Principal Display Panel (150 mL Bottle Label)

Label for Diclofenac Sodium Topical Solution 1.5% w/w, a prescription transdermal solution/drops, with NDC 76420-134-05. The label indicates a quantity of 150 units and states the product is a clear, colorless to faintly pink-orange solution. It is relabeled by Enovachem Pharmaceuticals and manufactured for Sircle Laboratories, LLC.*

* 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.