Main Timely review of notifications of new dietary ingredients impacts the public health by preventing substances that are not actually dietary ingredients from being used in dietary supplements, and assuring that new dietary ingredients have adequate evidence for presumption of safety. Since these statutory requirements are notifications rather than pre-market approvals, it is essential that ONLDS have completed review of the information before the submitter markets the product, to notify them of any safety or regulatory concerns before the product reaches consumers. <i>Information is current as of December 31, 2012.</i> Percentage column 0 100

FY 2010 6 Month Overall: 50%

Oct 2009 N/A Nov 2009 N/A Dec 2009 N/A Jan 2010 N/A Feb 2010 N/A Mar 2010 N/A Apr 2010 0 May 2010 29 Jun 2010 60 Jul 2010 60 Aug 2010 100 Sep 2010 N/A 0 100

FY 2011 Overall: 70%

Oct 2010 80 Nov 2010 100 Dec 2010 67 Jan 2011 75 Feb 2011 75 Mar 2011 67 Apr 2011 87 May 2011 0 Jun 2011 67 Jul 2011 50 Aug 2011 100 Sep 2011 75

FY 2012 Overall: 80%

Oct 2011 100 Nov 2011 80 Dec 2011 75 Jan 2012 100 Feb 2012 50 Mar 2012 100 Apr 2012 83 May 2012 50 Jun 2012 100 Jul 2012 83 Aug 2012 67 Sep 2012 67

FY 2013 YTD: 79%

Oct 2012 N/A Nov 2012 75% Dec 2012 83% Jan 2013 Feb 2013 Mar 2013 Apr 2013 May 2013 Jun 2013 Jul 2013 Aug 2013 Sep 2013 http://www.fda.gov/AboutFDA/Transparency/track/ucm206221.htmFDA-TRACK CFSAN Dashboard ਍††਍਍਍਍਍਍਍