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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>7</VOL>
    <DATE>2010-04-01</DATE>
    <ORIGINALDATE>2010-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Table Of Contents</TITLE>
    <GRANULENUM/>
    <ANCESTORS>
      <PARENT HEADING="Title 21" SEQ="1">Food and Drugs</PARENT>
      <PARENT HEADING="CHAPTER I" SEQ="0">FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)</PARENT>
    </ANCESTORS>
  </FDSYS>
  <TOC>
    <TOCHD>
      <PRTPAGE P="3"/>
      <HD SOURCE="HED">CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)</HD>
    </TOCHD>
    <EDNOTE>
      <HD SOURCE="HED">Editorial Note:</HD>
      <P>Nomenclature changes to chapter I appear at 59 FR 14366, Mar. 28, 1994, and 66 FR 56035, Nov. 6, 2001.</P>
    </EDNOTE>
    <SUBCHAP>
      <HD SOURCE="HED">SUBCHAPTER F—BIOLOGICS</HD>
    </SUBCHAP>
    <PTHD>Part</PTHD>
    <PGHD>Page</PGHD>
    <CHAPTI>
      <PT>600</PT>
      <SUBJECT>Biological products: general</SUBJECT>
      <PG>5</PG>
      <PT>601</PT>
      <SUBJECT>Licensing</SUBJECT>
      <PG>21</PG>
      <PT>606</PT>
      <SUBJECT>Current good manufacturing practice for blood and blood components</SUBJECT>
      <PG>48</PG>
      <PT>607</PT>
      <SUBJECT>Establishment registration and product listing for manufacturers of human blood and blood products</SUBJECT>
      <PG>61</PG>
      <PT>610</PT>
      <SUBJECT>General biological products standards</SUBJECT>
      <PG>67</PG>
      <PT>630</PT>
      <SUBJECT>General requirements for blood, blood components, and blood derivatives</SUBJECT>
      <PG>95</PG>
      <PT>640</PT>
      <SUBJECT>Additional standards for human blood and blood products</SUBJECT>
      <PG>96</PG>
      <PT>660</PT>
      <SUBJECT>Additional standards for diagnostic substances for laboratory tests</SUBJECT>
      <PG>120</PG>
      <PT>680</PT>
      <SUBJECT>Additional standards for miscellaneous products</SUBJECT>
      <PG>132</PG>
    </CHAPTI>
    <SUBCHAP>
      <HD SOURCE="HED">SUBCHAPTER G—COSMETICS</HD>
    </SUBCHAP>
    <CHAPTI>
      <PT>700</PT>
      <SUBJECT>General</SUBJECT>
      <PG>136</PG>
      <PT>701</PT>
      <SUBJECT>Cosmetic labeling</SUBJECT>
      <PG>144</PG>
      <PT>710</PT>
      <SUBJECT>Voluntary registration of cosmetic product establishments</SUBJECT>
      <PG>157</PG>
      <PT>720</PT>
      <SUBJECT>Voluntary filing of cosmetic product ingredient composition statements</SUBJECT>
      <PG>158</PG>
      <PT>740</PT>
      <SUBJECT>Cosmetic product warning statements</SUBJECT>
      <PG>162</PG>
      <PT>741-799</PT>
      <RESERVED>[Reserved]</RESERVED>
    </CHAPTI>
  </TOC>
</CFRGRANULE>
