Diclofenac Sodium
Product Images NDC 76074-501

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 76074-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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FDA Label Image

Medi-sulting-diclofenac Label Rx Ndc-1 (Medi Sulting Diclofenac Label Rx Ndc 1)

Medi-sulting-diclofenac Label Rx Ndc-1 (Medi Sulting Diclofenac Label Rx Ndc 1)
Diclofenac Sodium Gel 3% is an ophthalmic solution used to treat active keratosis. The gel should be applied to the affected area and smoothed gently into the skin, or as prescribed by a physician. The usual duration of treatment is from 60 to 90 days. The gel contains 30 mg/g of Diclofenac Sodium and inactive ingredients like Hyaluronate Sodium, Benzyl Alcohol, Polyethylene Glycol Monomethyl Ether, and Purified water. The drug should be kept away from children and stored between 20 to 25 degrees Celsius. For full prescribing information, refer to the package insert. The manufacturer of the drug is Medi-Sulting, LLC located in San Jose, CA. Contact Medi-Sulting.com or call 888 907-2833 for further information. NDC 76074 501 11.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.