Product Images Diclofenac Sodium

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Product Label Images

The following 8 images provide visual information about the product associated with Diclofenac Sodium NDC 13107-269 by Aurolife Pharma Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Figure A - diclofenac fig1

Figure A - diclofenac fig1

Figure B. - diclofenac fig2

Figure B. - diclofenac fig2

Figure C. - diclofenac fig3

Figure C. - diclofenac fig3

Figure D. - diclofenac fig4

Figure D. - diclofenac fig4

Figure E. - diclofenac fig5

Figure E. - diclofenac fig5

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 2% w/w Container Label (112 g Bottle - diclofenac fig6

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 2% w/w Container Label (112 g Bottle - diclofenac fig6

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 fig7

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 2% w/w Container Carton Label (112 g Bottle) - diclofenac fig7

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

Chemical Structure - diclofenac str

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.