Fenovar Kit
Product Images NDC 72835-202

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Fenovar (NDC 72835-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by V2 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.

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Image Description (Fenovar Packaging)

Fenovar is a muscle pain relieving cream that comes in a 55-gram tube with an NDC number of 72835-202-02. It is a topical solution for skin usage.*

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Muscle Rub Image 1 (B5109d5c 7849 46b3 9bd6 44eac11ba556 01)

This is a description of a pain relief product with the NDC code 45802-174-53 that provides fast relief from minor arthritis, backache, muscle and joint pain. It is a pain-relieving cream that is greaseless and comes in a 30Z package. The active ingredients can be compared to that of Bengay, and if prescribed by a doctor, it may be covered by FSA or HSA accounts, private health plans, Medicaid/Medicare. The text also mentions reducing costs through drug formularies.*

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Muscle Rub Image 2 (B5109d5c 7849 46b3 9bd6 44eac11ba556 02)

This is a drug facts label for a greaseless pain relieving cream. It contains two active ingredients, Mantfol 108 and Nethyl aioje 15%, which serve as topical analgesics. It should only be used externally and not applied to wounds, damaged skin, or mucous membranes. If used by children under 12 or symptoms last more than seven days, a doctor should be consulted. Keep out of reach of children and if swallowed seek medical attention. Each tube contains 30 oz of cream. Contact 1800-719-280 for any questions or comments.*

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Structural Formula (Diclofenac Sodium Topical Solution 1)

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Figure A1 (Diclofenac Sodium Topical Solution 2)

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Figure A2 (Diclofenac Sodium Topical Solution 3)

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Figure B (Diclofenac Sodium Topical Solution 4)

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Figure C (Diclofenac Sodium Topical Solution 5)

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Label (Diclofenac Sodium Topical Solution 6)

This is a warning and usage statement for Amneal Pharmaceuticals' Diclofenac Sodium Topical Solution. The solution should be applied to clean, dry skin and should be allowed time to dry before allowing contact with other people or surfaces. The hands should be washed after application. If persistent skin irritation develops, usage should be discontinued and a physician consulted. The mixture includes several excipients, including alcohol and glycerin, and should be stored between 20-25°C. The solution should not come into contact with eyes or mucous membranes, and the dosage is indicated as 40 drops, four times a day.*

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Carton (Diclofenac Sodium Topical Solution 7)

* 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.