Diclofenac Sodium Gel
Product Images NDC 68788-7772

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 68788-7772). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred 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.

FDA Label Image

Diclofenac Sodium Topical Gel 1% (Diclo Carton)

Diclofenac Sodium Topical Gel 1% is a generic medication for Voltaren. It contains 1% weight in weight of diclofenac sodium, USP. It is manufactured by Encube Ethicals Private Limited and is available in different package sizes. The medication must be stored at a temperature of 68 to 77°F (20° to 25°C) and kept away from the reach of children. The drug is to be applied externally twice a day, and transfer of the medication to any person other than the patient for whom it was prescribed is prohibited by Federal law. NDC, Lot#, and Batch# are some of the identification numbers marked on the packaging for inventory purposes. More information and directions are available in English.*

FDA Label Image

Dosing-card.jpg (Dosing Card)

This is a dosing card for Diclofenac Sodium Topical Gel, 1% that is used for 100g tube. The card has a length of 2.25 inches and a width of 4.5 inches. The instructions for use should be consulted before use.*

FDA Label Image

Figure- .jpg (Figure Gei)

FDA Label Image

Step.jpg (Step)

FDA Label Image

Structure.jpg (Structure)

This text is not enough to generate a useful description. It appears to be chemical symbols or formulas, but there is not enough context to provide meaning. The text reads "cl, NH, ONa*, cl."*

* 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.