Diclofenac Sodium
Product Images NDC 50090-2787

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 50090-2787). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 Sodium Topical Gel 1 Percent Rx 1)

FDA Label Image

Dosing Card Figure A (Diclofenac Sodium Topical Gel 1 Percent Rx 2)

Dosing Card Figure A (Diclofenac Sodium Topical Gel 1 Percent Rx 2)
This is a dosing card for Diclofenac Sodium Topical Gel 1%. It indicates the amount of gel to be used, either 2 grams or 4 grams, with corresponding measurements of 2.25 inches and 4.5 inches. Instructions for use are also available.*
FDA Label Image

Figure B (Diclofenac Sodium Topical Gel 1 Percent Rx 3)

FDA Label Image

Figure C (Diclofenac Sodium Topical Gel 1 Percent Rx 4)

FDA Label Image

Figure D (Diclofenac Sodium Topical Gel 1 Percent Rx 5)

FDA Label Image

Figure E (Diclofenac Sodium Topical Gel 1 Percent Rx 6)

FDA Label Image

Figure F (Diclofenac Sodium Topical Gel 1 Percent Rx 7)

FDA Label Image

Figure G (Diclofenac Sodium Topical Gel 1 Percent Rx 8)

FDA Label Image

Label Image (Lbl500902787)

Label Image (Lbl500902787)
This text is not enough to generate a useful description. It appears to refer to a topical gel with a concentration of 1%, and a numeric code of 1006. However, there is no indication of what the gel is used for, its name, manufacturer, or any other relevant information.*

* 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.