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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>7</VOL>
    <DATE>2002-04-01</DATE>
    <ORIGINALDATE>2002-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Table Of Contents</TITLE>
    <GRANULENUM>I</GRANULENUM>
    <HEADING>CHAPTER I</HEADING>
    <ANCESTORS>
      <PARENT HEADING="Title 21" SEQ="0">Food and Drugs</PARENT>
    </ANCESTORS>
  </FDSYS>
  <CFRTOC>
    <PTHD>
      <E T="03">Part</E>
    </PTHD>
    <CHAPTI>
      <SUBJECT>
        <E T="04">chapter i</E>—Food and Drug Administration, Department of Health and Human Services (Continued)</SUBJECT>
      <PG>600</PG>
    </CHAPTI>
    <CROSSREF>
      <HD SOURCE="HED">Cross References:</HD>
      <P>Food Safety and Inspection Service, Department of Agriculture: See 9 CFR Chapter III.</P>
      <P>Federal Trade Commission: See Commercial Practices, 16 CFR Chapter I.</P>
      <P>U.S. Customs Service, Department of the Treasury: See Customs Duties, 19 CFR Chapter I.</P>
      <P>Internal Revenue Service, Department of the Treasury: See Internal Revenue, 26 CFR Chapter I.</P>
      <P>Bureau of Alcohol, Tobacco, and Firearms, Department of the Treasury: See Alcohol, Tobacco Products and Firearms, 27 CFR Chapter I.</P>
    </CROSSREF>
  </CFRTOC>
  <CHAPTER>
    <TOC>
      <TOCHD>
        <PRTPAGE P="3"/>
        <HD SOURCE="HED">CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)</HD>
        <P>(Parts 600-799)</P>
      </TOCHD>
      <EDNOTE>
        <HD SOURCE="HED">Editorial Note:</HD>
        <P>For nomenclature changes to chapter I see 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>19</PG>
        <PT>606</PT>
        <SUBJECT>Current good manufacturing practice for blood and blood components</SUBJECT>
        <PG>42</PG>
        <PT>607</PT>
        <SUBJECT>Establishment registration and product listing for manufacturers of human blood and blood products</SUBJECT>
        <PG>54</PG>
        <PT>610</PT>
        <SUBJECT>General biological products standards</SUBJECT>
        <PG>60</PG>
        <PT>630</PT>
        <SUBJECT>General requirements for blood, blood components, and blood derivatives</SUBJECT>
        <PG>84</PG>
        <PT>640</PT>
        <SUBJECT>Additional standards for human blood and blood products</SUBJECT>
        <PG>85</PG>
        <PT>660</PT>
        <SUBJECT>Additional standards for diagnostic substances for laboratory tests</SUBJECT>
        <PG>109</PG>
        <PT>680</PT>
        <SUBJECT>Additional standards for miscellaneous products</SUBJECT>
        <PG>122</PG>
      </CHAPTI>
      <SUBCHAP>
        <HD SOURCE="HED">SUBCHAPTER G—COSMETICS</HD>
      </SUBCHAP>
      <CHAPTI>
        <PT>700</PT>
        <SUBJECT>General</SUBJECT>
        <PG>126</PG>
        <PT>701</PT>
        <SUBJECT>Cosmetic labeling</SUBJECT>
        <PG>132</PG>
        <PT>710</PT>
        <SUBJECT>Voluntary registration of cosmetic product establishments</SUBJECT>
        <PG>145</PG>
        <PT>720</PT>
        <SUBJECT>Voluntary filing of cosmetic product ingredient  composition statements</SUBJECT>
        <PG>146</PG>
        <PT>740</PT>
        <SUBJECT>Cosmetic product warning statements</SUBJECT>
        <PG>150</PG>
        <PT>741-799</PT>
        <RESERVED>[Reserved]</RESERVED>
      </CHAPTI>
    </TOC>
  </CHAPTER>
</CFRGRANULE>
