The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 2006 - Administrative law The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
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Page 9
... proposed findings if section 5 ( b ) of the Fair Packaging and Labeling Act applies , pursuant to parts 10 , 12 , 13 , 14 , 15 , 16 , and 19 of this chapter . §1.24 Exemptions from required label statements . The following exemptions ...
... proposed findings if section 5 ( b ) of the Fair Packaging and Labeling Act applies , pursuant to parts 10 , 12 , 13 , 14 , 15 , 16 , and 19 of this chapter . §1.24 Exemptions from required label statements . The following exemptions ...
Page 14
... proposals for bringing the article into compliance with the act or rendering it other than a food , drug , device , or cosmetic . ( b ) Specify the time and place where such operations will be carried out and the approximate time for ...
... proposals for bringing the article into compliance with the act or rendering it other than a food , drug , device , or cosmetic . ( b ) Specify the time and place where such operations will be carried out and the approximate time for ...
Page 48
... proposed decision , with a statement of reasons . The hearing participant may review and comment on the presiding officer's report within 4 hours of issuance of the report . The presiding officer will then issue the final agency ...
... proposed decision , with a statement of reasons . The hearing participant may review and comment on the presiding officer's report within 4 hours of issuance of the report . The presiding officer will then issue the final agency ...
Page 55
... proposed labeling is intended for use only with an approved individually specified drug , device , or biological product where both are required to achieve the intended use , indication , or effect and where upon approval of the proposed ...
... proposed labeling is intended for use only with an approved individually specified drug , device , or biological product where both are required to achieve the intended use , indication , or effect and where upon approval of the proposed ...
Page 56
... proposed labeling is for use only with another individually specified investigational drug , device , or biological product where both are required to achieve the intended use , indication , or effect . ( f ) Device has the meaning ...
... proposed labeling is for use only with another individually specified investigational drug , device , or biological product where both are required to achieve the intended use , indication , or effect . ( f ) Device has the meaning ...
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Common terms and phrases
acid action addi administrative record advisory committee agency amended amounts consistent application approval article of food authorized Canthaxanthin chapter clinical investigation cluding color additive D&C Color additive mixtures coloring foods coloring purposes Commissioner conform in identity conformity assessment contain Cosmetic Act D&C Orange D&C Red D&C Yellow determination device diluents Division of Dockets Dockets Management Drug Administration drug application electronic employee Exemption from certification externally applied drugs facility FD&C Federal Acquisition Regulation Federal Food FEDERAL REGISTER filed food additive Food and Drug hearing Identity and specifications issue Lead as Pb lic health listed manufacturing practice matter ment metics mixtures for coloring mixtures prepared therefrom naphthalenedisulfonic notify paragraph participation party percent person petition presiding officer procedures public disclosure regulations regulatory request restrictions safely salt Service submission submitted subpart tice tification tion tive Total color
Popular passages
Page 247 - ... a drug and the methods used in, or the facilities or controls used for, its manufacture, processing, packing, or holding do not conform to or are not operated or administered in conformity with current good manufacturing practice...
Page 322 - ... color additive" means a material which— (A) is a dye, pigment, or other substance made by a process of synthesis or similar artifice, or extracted, isolated, or otherwise derived, with or without intermediate or final change of identity, from a vegetable, animal, mineral, or other source, and...
Page 181 - Although relevant, evidence may be excluded if its probative value is substantially outweighed by the danger of unfair prejudice, confusion of the issues, or misleading the jury, or by considerations of undue delay, waste of time, or needless presentation of cumulative evidence.
Page 475 - X Office of Community Services, Administration for Children and Families, Department of Health and Human Services (Parts 1000—1099) XI National Foundation on the Arts and the Humanities (Parts...
Page 231 - Provided, however , that if any individual is denied any right, privilege, or benefit that he would otherwise be entitled "by Federal law, or for which he would otherwise be eligible, as a result of the maintenance of such material, such material shall be provided to such individual...
Page 285 - ... rights, and whom to contact in the event of a research-related injury to the subject; and (8) A statement that participation is voluntary, refusal to participate will Involve no penalty or loss of benefits to which the subject is otherwise entitled...
Page 77 - advisory committee" means any committee, board, commission, council, conference, panel, task force, or other similar group, or any subcommittee or other subgroup thereof...
Page 293 - food additive" means any substance the intended use of which results or may reasonably be expected to result, directly or indirectly, in its becoming a component or otherwise affecting the characteristics of any food...
Page 407 - HALDOL tablets contain FD&C Yellow No 5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals, especially in those who have...
Page 235 - The Congress authorizes and directs that, to the fullest extent possible: (1) the policies, regulations, and public laws of the United States shall be interpreted and administered in accordance with the policies set forth in this Act...