0910-AF95 200710 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Status of Certain Additional Over-the-Counter Drug Category II Active Ingredients Routine and Frequent Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 201 21 CFR 310 21 CFR 330 to 358 21 USC 321p 21 USC 331 21 USC 351 to 353 21 USC 355 21 USC 360 21 USC 360a 21 USC 371 21 USC 371a No NPRM 06/00/2008 No No Local State Yes No Not Collected Walter Ellenberg J. 0910 Food and Drug Administration FDA 301 796-2090 301 796-9899 walter.ellenberg@fda.hhs.gov Center for Drug Evaluation and Research, WO-22, Room 5488, 10903 New Hampshire Avenue, Silver Spring MD 20993