Voltaren
Product Images NDC 50436-3621

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Voltaren (NDC 50436-3621). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Structure (Image 01)

Structure (Image 01)
Chemical structure diagram depicting the molecular structure of the active ingredient in Voltaren as represented by the sodium salt form, showing chlorine atoms and a carboxylate group attached to an aromatic ring system.*
FDA Label Image

Figure 1 (Image 02)

Figure 1 (Image 02)
Dosing card for Voltaren Gel (diclofenac sodium topical gel) 1%. The card is marked to measure 2 grams (2.25 inches) and 4 grams (4.5 inches) quantity dispensed. The labeler is Unit Dose Services, product NDC 50436-3621.*
FDA Label Image

Figure 2 (Image 03)

Figure 2 (Image 03)
Illustrations showing application instructions for Voltaren. Figure B depicts dispensing gel onto the skin. Figure C shows rubbing the gel into the skin with one hand using a cloth or tissue. Figure D demonstrates massaging the gel into the skin with circular motions using fingers or palms.*
FDA Label Image

Figure 3 (Image 04)

Figure 3 (Image 04)
Illustrations labeled Figure E, F, and G showing the application process of a topical gel. Figure E depicts a dosing card for Voltaren gel. Figure F shows applying the gel to the skin with a dosing card or similar device. Figure G illustrates rubbing the gel into the skin, focusing on the knee area.*
FDA Label Image

Label Image (Lbl504363621)

Label Image (Lbl504363621)
Voltaren Gel 1% (diclofenac sodium) topical gel, 100 gm unit dose packaging. Label includes storage instructions, manufacturing information by Novartis Consumer Health, Inc., and NDC 50436-3621-1. Several lot and expiration placeholders are shown.*

* 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.