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J Am Acad Dermatol. 2007 Nov;57(5):854-72. Epub 2007 Apr 27.

The safety of hydroquinone: a dermatologist's response to the 2006 Federal Register.

Author information

1
Department of Dermatology, The Mount Sinai Medical Center, New York City, USA. TARONY@aol.com

Abstract

Recently, the US Food and Drug Administration proposed a ban on over-the-counter hydroquinone mainly on the basis of high absorption, reports of exogenous ochronosis in humans, and murine hepatic adenomas, renal adenomas, and leukemia with large doses over extended time periods. Systemic exposure to hydroquinone from routine topical application is no greater than that from quantities present in common foods. While murine hepatic adenomas increased, murine hepatocellular carcinomas decreased, suggesting a protective effect. Renal tumors are sex, species, and age specific and therefore do not appear relevant to humans after decades of widespread use. Murine leukemia has not been reproducible and would not be expected from small topical doses. Finally, a literature review of exogenous ochronosis and clinical studies employing hydroquinone (involving over 10,000 exposures under careful clinical supervision) reveal an incidence of exogenous ochronosis in the United States of 22 cases in more than 50 years. Therefore, the proposed ban appears to be unnecessarily extreme.

PMID:
17467115
DOI:
10.1016/j.jaad.2007.02.020
[Indexed for MEDLINE]

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