The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 1974 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. |
No grāmatas satura
1.5. rezultāts no 16.
vi. lappuse
... Director , Office of the Federal Register , National Archives and Records Service , General Services Administration , Washington , D.C. 20408. Sales are handled exclusively by the Superintendent of Documents , Government Printing Office ...
... Director , Office of the Federal Register , National Archives and Records Service , General Services Administration , Washington , D.C. 20408. Sales are handled exclusively by the Superintendent of Documents , Government Printing Office ...
60. lappuse
... director " means the director of the district of the Food and Drug Administration having juris- diction over the port of entry through which an article is imported or offered for import , or such officer of the district as he may ...
... director " means the director of the district of the Food and Drug Administration having juris- diction over the port of entry through which an article is imported or offered for import , or such officer of the district as he may ...
61. lappuse
... director may grant such additional time as he deems necessary . ( c ) An authorization may be amended upon a showing of reasonable grounds therefor and the filling of an amended application for authorization with the district director ...
... director may grant such additional time as he deems necessary . ( c ) An authorization may be amended upon a showing of reasonable grounds therefor and the filling of an amended application for authorization with the district director ...
75. lappuse
... Directors and Deputy Director of Bureaus , the Asso- ciate Director for Regulatory and Admin- istrative Management of the Bureau of Biologics , Regional Food and Drug Di- rectors , and Deputy Regional Food and Drug Directors are ...
... Directors and Deputy Director of Bureaus , the Asso- ciate Director for Regulatory and Admin- istrative Management of the Bureau of Biologics , Regional Food and Drug Di- rectors , and Deputy Regional Food and Drug Directors are ...
76. lappuse
... Director and Deputy Director of the Bureau of Radiological Health , and the Director of the Division of Com- pliance of that Bureau are authorized to request , under section 360 ( a ) of the Public Health Service Act , from the Sec ...
... Director and Deputy Director of the Bureau of Radiological Health , and the Director of the Division of Com- pliance of that Bureau are authorized to request , under section 360 ( a ) of the Public Health Service Act , from the Sec ...
Citi izdevumi - Skatīt visu
Bieži izmantoti vārdi un frāzes
0.2 percent 52 Stat acid Added advertisement amended annatto antibiotic authorized batches thereof bear Bureau cent chapter chlorcyclizine Chlorides and sulfates color additive mixtures coloring foods coloring purposes Commissioner of Food conform containing Cosmetic Act cyclizine D&C Red declaration Department diluents Director and Deputy dosage unit Drug Administration dye as determined Effective date Exemption from certification FD&C Federal Food FEDERAL REGISTER filing flavor fluid ounce Food and Drug hexachlorophene ingredient Labeling requirements listed manufacturing practice matter at 135 ment metic milligrams misbranded mixtures for coloring new-drug application oleomargarine package Packaging and Labeling paragraph petition prepared therefrom principal display panel proprietary name public health Pure dye quantity of contents regulations request restrictions Revised safe salt section 401 shipment standards of identity statement straight color subparagraph Subpart substance thereof are exempt tion titanium dioxide titanium trichloride titration with titanium vitamin Volatile matter
Populāri fragmenti
141. lappuse - ... 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...
52. lappuse - Labeling on or within the package from which the drug is to be dispensed bears adequate information for its use, including indications, effects, dosages, routes, methods, and fre-quency and duration of administration, and any relevant hazards, contraindications, side effects, and precautions under which practitioners licensed by law to administer the drug can use the drug safely and for the purposes for which it is intended, including all purposes for which it is advertised or represented...
54. lappuse - ... because of its toxicity or other potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use, is not safe for use except under the supervision of a practitioner licensed by law to administer such drug...
137. lappuse - Code, and shall accompany the proposal through the existing agency review processes; (D) study, develop, and describe appropriate alternatives to recommended courses of action in any proposal which involves unresolved conflicts concerning alternative uses of available resources...
69. lappuse - When portions only of a document are to be relied upon, the offering party shall prepare the pertinent excerpts, adequately identified, and shall supply copies of such excerpts, together with a statement indicating the purpose for which such materials will be offered, to the hearing examiner and to the other parties.
6. lappuse - label" means a display of written, printed, or graphic matter upon the immediate container of any article ; and a requirement made by or under authority of this Act that any word, statement, or other information appear on the label shall not be considered to be complied with unless such word, statement, or other information also appears on the outside container or wrapper, if any there be, of the retail package of such article, or is easily legible through the outside container or wrapper. (1) The...
145. lappuse - ... and the cumulative effect, if any, of such additive in the diet of man or animals, taking into account the same or any chemically or pharmacologically related substance or substances in the diet including, but not limited to food additives and pesticide chemicals for which tolerances or exemptions from tolerances have been established.
89. lappuse - The same information concerning the ingredients of the drug as appears on the label and labeling on or within the package from which the drug is to be dispensed...
19. lappuse - ... required by or under authority of the act to appear on the label; (5) Insufficiency of label space (for the prominent placing of such word, statement, or information) resulting from the use of label space to give materially greater conspicuousness to any other word, statement, or information, or to any design or device; or (в) Smallness or style of type In which such word, statement, or information appears, insufficient background contrast, obscuring designs or vignettes, or crowding with other...
70. lappuse - If a party objects to the admission or rejection of any evidence or to the limitation of the scope of any examination or cross-examination, he shall state briefly the grounds of such objection, whereupon an automatic exception will follow if the objection is overruled by the presiding officer. The transcript shall not include argument or debate thereon, except as ordered by the presiding officer.