<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="cfr.xsl"?>
<CFRGRANULE xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:noNamespaceSchemaLocation="CFRMergedXML.xsd">
  <FDSYS>
    <CFRTITLE>16</CFRTITLE>
    <CFRTITLETEXT>Commercial Practices</CFRTITLETEXT>
    <VOL>2</VOL>
    <DATE>2004-01-01</DATE>
    <ORIGINALDATE>2004-01-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Marketing history.</TITLE>
    <GRANULENUM>1702.14</GRANULENUM>
    <HEADING>Section 1702.14</HEADING>
    <ANCESTORS>
      <PARENT HEADING="Title 16" SEQ="3">Commercial Practices</PARENT>
      <PARENT HEADING="CHAPTER II" SEQ="2">CONSUMER PRODUCT SAFETY COMMISSION</PARENT>
      <PARENT HEADING="SUBCHAPTER E" SEQ="1">POISON PREVENTION PACKAGING ACT OF 1970 REGULATIONS</PARENT>
      <PARENT HEADING="PART 1702" SEQ="0">PETITIONS FOR EXEMPTIONS FROM POISON PREVENTION PACKAGING ACT REQUIREMENTS; PETITION PROCEDURES AND REQUIREMENTS</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 1702.14</SECTNO>
    <SUBJECT>Marketing history.</SUBJECT>
    <P>Each petition for an exemption under this part shall include a statement of the marketing history of the substance for which an exemption is requested. The marketing history dates from the year in which each form of the product was introduced onto the market. The marketing history shall include the total number of units of each form or strength and package size of the product distributed since the product was introduced onto the market. In the case of prescription drugs, the average prescription size for the product should also be indicated, if known.</P>
  </SECTION>
</CFRGRANULE>
