2005N-0345 Drug Approvals: Circumstances under which an active ingredient may be simultaneously marketed in both a prescription drug product and an over-the-counter drug product
FDA Comment Number : EC722
Submitter : Mr. Wendell Neugebauer Date & Time: 10/12/2005 06:10:47
Organization : Mr. Wendell Neugebauer
Category : International Public Citizen
Issue Areas/Comments
The World Health Organization has declared that oral contraceptives are a Group 1 carcinogen (Press Release #167, July 29, 2005).
The FDA should not approve of the morning after pill (a.k.a. Plan B, emergency contraception) or contraceptives in general, either by prescription or OTC.

Why should the FDA recommend a carcinogen?