Figure A (Diclofenac Fig1)
Diclofenac Sodium Solution
Product Images NDC 13107-269
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 13107-269). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Aurolife Pharma Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Figure B. (Diclofenac Fig2)
Figure C. (Diclofenac Fig3)
Figure D. (Diclofenac Fig4)
Figure E. (Diclofenac Fig5)
Package Label-principal Display Panel (2% w/w Container Label (112 g Bottle)
This is a prescription medication called Diclofenac Sodium Topical Solution. It is used for external use only and has an alcohol content of 31.07% v/v. The usual dosage is to apply two pump activations to the affected knee(s) two times a day. Each pump activation of the 3.8FL.0Z. (112 grams) product delivers 1 gram of solution (20 mg diclofenac sodium USP). This medication should not be used near the eyes or mucous membranes, and hands should be thoroughly washed after application. If persistent skin irritation develops, discontinue use of the product and consult a physician. The medication contains dimethyl sulfoxide, ethanol 96%, hydroxypropyl cellulose, propylene glycol, and purified water as excipients. The medication should be stored at 20° to 25°C (68° to 77°F). The manufacturer is Aurobindo Pharma USA, Inc. The text also includes a warning to see the package insert for complete prescribing information.*
Package Label-principal Display Panel (2% w/w Container Carton Label (112 g Bottle))
Diclofenac Sodium Topical Solution is a USP prescribed for external use only. With an alcohol content of 31.07% v/v, it must be applied to clean, dry skin. In case of persistent skin irritation, stop using the product and seek consultation from a doctor. The solution consisting of diclofenac sodium USP (20mg), and other excipients such as dimethyl sulfoxide, ethanol 96%, hydroxypropy! cellulose, propylene glycol, and purified water, must be stored at controlled room temperature as directed in the USP. This drug should be dispensed with an enclosed medication guide to each patient by the pharmacist. The usual dosage is to pump the solution twice and apply it to two affected knee areas twice daily.*
Chemical Structure (Diclofenac Str)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
