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Diclofenac Sodium Gel
Product Images NDC 0472-1783
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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 0472-1783). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Actavis Pharma, 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.
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1 (Image 2)
Diclofenac Sodium Gel 3% is a topical medication used for the treatment of actinic keratosis. It contains diclofenac sodium USP, along with other inactive ingredients such as benzyl alcohol and purified water. The recommended adult dosage is 0.5 g applied to affected skin, smoothed in gently. The usual duration of therapy is between 60 to 90 days. Caution must be taken as it is for external use only, and is not to be used for ophthalmic purposes. The gel is to be stored between temperatures of 20°C to 25°C, with excursions between 15°C to 30°C. It must be protected from heat and should not be frozen. It must be kept out of the reach of children. A medication guide must be dispensed to each patient by the pharmacist.*
* 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.
