"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
Apply a thin film of Pandel (hydrocortisone probutate cream) Cream, 0.1% to the affected area once or twice a day depending on the severity of the condition. Massage gently until the medication disappears.
As with other corticosteroids, therapy should be discontinued when control is achieved. If no improvement is seen within 2 weeks, reassessment of the diagnosis may be necessary. Pandel (hydrocortisone probutate cream) Cream, 0.1% should not be used with occlusive dressings unless directed by the physician. Pandel (hydrocortisone probutate cream) Cream, 0.1% should not be applied in the diaper area, as diapers or plastic pants may constitute occlusive dressings.
Pandel (hydrocortisone probutate cream) Cream, 0.1%, a white to off-white opaque cream is supplied as follows:
15 gtubes NDC 64682-200-15
45 g tubes NDC 64682-200-46
80 g tubes NDC 64682-200-80
Store at controlled room temperature 15°-30°C (59°-86°F).
Manufactured for: CollaGenex Pharmaceuticals, Inc. Newtown, PA 18940 by Altana Inc., Melville, New York 11747. FDA revision date: 2/28/1997
Last reviewed on RxList: 6/24/2008
This monograph has been modified to include the generic and brand name in many instances.
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