Image (4ea8a24a B7ad 4db3 B664 B5a5c938010c 01)
Diclofenac Sodium Gel
Product Images NDC 62332-581
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 62332-581). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Alembic Pharmaceuticals 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.
Container Label (4ea8a24a B7ad 4db3 B664 B5a5c938010c 02)
This is a medication with the NDC code 62332-581-31. It is a Diclofenac Sodium Topical Gel for external use only. The product contains 30 mg of diclofenac sodium per gram and is manufactured by Alembic Pharmaceuticals. It also has inactive ingredients that include sodium hyaluronate, benzyl alcohol, and purified water. The recommended adult dosage is applying 0.5 g of gel twice a day. The medication should be stored at a controlled room temperature and kept out of the reach of children. The lot number and expiry date can be found below the crimp of the tube.*
Carton Label (4ea8a24a B7ad 4db3 B664 B5a5c938010c 03)
Diclofenac Sodium Topical Gel is an external use ointment with active ingredient Diclofenac Sodium that comes in a 100g package with inactive components such as Sodium hyaluronate, benzyl alcohol, polyethylene glycol monomethyl ether, and purified water. The recommended use is to apply 0.5g of gel twice a day to affected areas. Ophthalmic use is prohibited. The product is produced by Alembic Pharmaceuticals, Inc. in Bedminster, NJ and Aleor Dermaceuticals Ltd., M in Karakhadi, Vadodara, India, with a manufacturing license of G / 25/2216.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
