"Today, the U.S. Food and Drug Administration issued a proposed order that, if finalized, would reclassify sunlamp products and require labeling to include a recommendation designed to warn young people not to use these devices.
Overdosage by topical application of XERESE is unlikely because of minimal systemic exposure [see CLINICAL PHARMACOLOGY].
Last reviewed on RxList: 2/3/2014
This monograph has been modified to include the generic and brand name in many instances.
Additional Xerese Information
Report Problems to the Food and Drug Administration
Skin & Beauty
Get beauty tips and body treatments.