"Scientists at the National Institutes of Health report they have discovered in mouse studies that a small molecule released in the spinal cord triggers a process that is later experienced in the brain as the sensation of itch.
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 19380
Last reviewed on RxList: 8/9/2013
This monograph has been modified to include the generic and brand name in many instances.
Additional Cordran Cream Information
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