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DOSAGE AND ADMINISTRATION
For moist lesions, a small quantity of the cream should be rubbed gently into the affected areas 2 or 3 times a day. For dry, scaly lesions, the ointment is applied as a thin film to affected areas 2 or 3 times daily.
Therapy should be discontinued when control is achieved. If no improvement is seen within 2 weeks, reassessment of the diagnosis may be necessary.
Cordran® (flurandrenolide, USP) should not be used with occlusive dressings unless directed by a physician. Tight-fitting diapers or plastic pants may constitute occlusive dressings.
Cordran® SP Cream is supplied in aluminum tubes as follows:
Cordran® SP Cream, 0.025%
30 g (NDC 16110-034-30)
60 g (NDC 16110-034-60)
120 g (NDC 16110-034-12)
Cordran® SP Cream, 0.05%
15 g (NDC 16110-035-15)
30 g (NDC 16110-035-30)
60 g (NDC 16110-035-60)
120 g (NDC 16110-035-12)
Cordran® Ointment is supplied in aluminum tubes as follows:
Cordran® Ointment, 0.05%
15 g (NDC 16110-026-15)
30 g (NDC 16110-026-30)
60 g (NDC 16110-026-60)
Keep out of reach of children.
Keep tightly closed.
Protect from light.
Store at 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F) [See USP controlled room temperature.].
Revision: 07/2013. Manufactured by DPT Laboratories, San Antonio, TX 78215 For Aqua Pharmaceuticals, West Chester, PA 19380This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 8/9/2013
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