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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>3</VOL>
    <DATE>2001-04-01</DATE>
    <ORIGINALDATE>2001-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Thiamine mononitrate.</TITLE>
    <GRANULENUM>184.1878</GRANULENUM>
    <HEADING>Section 184.1878</HEADING>
    <ANCESTORS>
      <PARENT HEADING="Title 21" SEQ="4">Food and Drugs</PARENT>
      <PARENT HEADING="CHAPTER I" SEQ="3">FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)</PARENT>
      <PARENT HEADING="SUBCHAPTER B" SEQ="2">FOOD FOR HUMAN CONSUMPTION</PARENT>
      <PARENT HEADING="PART 184" SEQ="1">DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE</PARENT>
      <PARENT HEADING="Subpart B" SEQ="0">Listing of Specific Substances Affirmed as GRAS</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 184.1878</SECTNO>
    <SUBJECT>Thiamine mononitrate.</SUBJECT>
    <P>(a) Thiamine mononitrate (C<E T="52">12</E>H<E T="52">17</E>N<E T="52">5</E>O<E T="52">4</E>S, CAS Reg. No. 532-43-4) is the mononitrate salt of thiamine. It occurs as white crystals or a white crystalline powder and is prepared from thiamine hydrochloride by dissolving the hydrochloride salt in alkaline solution followed by precipitation of the nitrate half-salt with a stoichiometric amount of nitric acid.</P>
    <P>(b) The ingredient meets the specifications of the Food Chemicals Codex, 3d Ed. (1981), p. 325, which is incorporated by reference. Copies are available from the National Academy Press, 2101 Constitution Ave. NW., Washington, DC 20418, or available for inspection at the Office of the Federal Register, 800 North Capitol Street, NW., suite 700, Washington, DC 20408.</P>

    <P>(c) In accordance with § 184.1(b)(1), the ingredient is used in food with no limitation other than current good manufacturing practice. The affirmation of this ingredient as generally recognized as safe (GRAS) as a direct human food ingredient is based upon <PRTPAGE P="547"/>the following current good manufacturing practice conditions of use:</P>
    <P>(1) The ingredient is used as a nutrient supplement as defined in § 170.3(o)(20) of this chapter.</P>
    <P>(2) The ingredient is used in food at levels not to exceed current good manufacturing practice. Thiamine mononitrate may be used in infant formula in accordance with section 412(g) of the Federal Food, Drug, and Cosmetic Act (the Act) or with regulations promulgated under section 412(a)(2) of the Act.</P>
    <P>(d) Prior sanctions for this ingredient different from the uses established in this section do not exist or have been waived.</P>
    <CITA>[48 FR 55124, Dec. 9, 1983]</CITA>
  </SECTION>
</CFRGRANULE>
