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Exelderm 1% Cream 60 Gm By Ranbaxy Labs.

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Exelderm 1% Cream 60 Gm By Ranbaxy Labs.

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Exelderm 1% Cream 60 Gm By Ranbaxy Labs. This Item Requires A Valid Order From A Physician Licensed in USA. Item Number.:RXD4310801/RXB10009928
Size : 60 GM
Selling UoM : EA
NDC: 10631-0101-60
UPC Barcode : 310631101602
Supplier: 0050000845 RANBAXY LABS (RX)
Supplier Material : 010160
Generic Code : 007376 SULCONAZOLE NITRATE TOPICAL CREAM (G) 1
Fine Line Class : 850085008510 All Rx Products
Product Category : RX Pharmaceuticals
Product Type : BRX Branded RX

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Product Description.:

EXELDERM (sulconazole nitrate) SOLUTION, 1.0% is a broad-spectrum antifungal agent intended for topical application. Sulconazole nitrate, the active ingredient in EXELDERM SOLUTION, is an imidazole derivative with antifungal and antiyeast activity.

Sulconazole nitrate is a white to off-white crystalline powder with a molecular weight of 460.77. It is freely soluble in pyridine slightly soluble in ethanol, acetone, and chloroform and very slightly soluble in water. It has a melting point of about 130?C.

EXELDERM SOLUTION contains sulconazole nitrate 10 mg/mL in a solution of propylene glycol, poloxamer 407, polysorbate 20, butylated hydroxyanisole, and purified water, with sodium hydroxide and, if necessary, nitric acid added to adjust the pH.

INDICATIONS

EXELDERM (sulconazole nitrate) SOLUTION, 1.0% is a broad-spectrum antifungal agent indicated for the treatment of tinea cruris and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum, and Microsporum canis and for the treatment of tinea versicolor. Effectiveness has not been proven in tinea pedis (athlete's foot).

Symptomatic relief usually occurs within a few days after starting EXELDERM SOLUTION and clinical improvement usually occurs within one week.

SIDE EFFECTS

There were no systemic effects and only infrequent cutaneous adverse reactions in 370 patients treated with sulconazole nitrate solution in controlled clinical trials. Approximately 1% of these patients reported itching and 1% burning or stinging. These complaints did not usually interfere with treatment.