FDA Mandates New Warning for Nonoxynol 9 OTC Contraceptive Products
Label Must Warn Consumers Products Do Not Protect Against STDs and HIV/AIDS
December 18, 2007
The U.S. Food and Drug Administration (FDA) issued a final rule today that requires that manufacturers of over-the-counter (OTC) stand-alone vaginal contraceptive and spermicidal products containing the chemical ingredient nonoxynol 9 (N9) include a warning that the chemical N9 does not provide protection against infection from HIV (the virus that causes AIDS) or other sexually transmitted diseases (STDs).
Stand-alone spermicides include gels, foams, films, or inserts containing N9 that are used by themselves for contraception. Consumers can protect themselves from the transmission of STDs and HIV by practicing abstinence, being in a monogamous relationship where neither partner is infected, and using condoms consistently and correctly.
"FDA is issuing this final rule to correct misconceptions that the chemical N9 in these widely available stand-alone contraceptive products protects against sexually transmitted diseases, including HIV infection," said Janet Woodcock, M.D., FDA's deputy commissioner for scientific and medical programs, chief medical officer, and acting director of the Center for Drug Evaluation and Research (CDER). "Clinical research has shown that N9 provides no protection against sexually transmitted diseases to the woman if her sexual partner is infected with an STD pathogen or HIV."
In addition, FDA is requiring that the labels warn consumers that the chemical N9 in stand-alone vaginal contraceptives and spermicides can irritate the vagina and rectum, which may increase the risk of contracting HIV/AIDS from an infected partner.
In January 2003, FDA proposed new warning statements and other labeling information for these products after results from a major clinical study in Africa and Thailand showed that women using a contraceptive gel product containing N9 were not protected against HIV and other STDs and were at higher risk for HIV infection than women using a placebo gel. Because these and other studies have shown that use of products containing N9 cause vaginal and rectal irritation, which can heighten the chance of becoming infected with HIV from an infected partner, FDA's action is based on the need to protect the public health and empower consumers to make better informed decisions about the use of these products.
This rule is being finalized following a public comment period and a thorough analysis of information and views from consumers, health care providers, academicians and industry. FDA is requiring that labeling of OTC vaginal contraceptive/spermicidal products containing N9 bear the following warnings:
Other information in the new labeling includes:
FDA is issuing the final rule to provide a clear, consistent message that N9 is not effective in preventing HIV transmission, and that N9 may actually facilitate transmission of the disease for those who are at risk for HIV/AIDS. This final rule is consistent with FDA's draft guidance for N9 use with condoms.
The full text of the final rule is posted at www.fda.gov/OHRMS/DOCKETS/98fr/80n-0280-nfr0003.pdf
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