The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 2001 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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Common terms and phrases
50 milligrams acervulina acid Administer Amount ampicillin Amprolium animal drug animal feed application approved bacitracin bacterial Bambermycins body weight Broiler chickens brunetti cattle caused by Eimeria chapter chlortetracycline coccidiosis coccidiosis caused coli Conditions of use-(1 contains continuously as sole daily days before slaughter dose erinarian Federal law restricts Feed continuously feeding practice Fenbendazole gentamicin grams grams per pound hydrochloride improved feed efficiency Indications infections intramuscularly labeling lasalocid licensed veterinarian Limitations lincomycin manufac medicated feed melengestrol acetate ment milligrams milligrams per pound milliliter mivati monensin necatrix neomycin Oesophagostomum oral oxytetracycline paragraph percent pound of body prevention of coccidiosis Product rate of weight recognized as safe Related tolerances residues restricts this drug revised roundworms roxarsone sodium sole ration sole source Specifications Sponsor strongyles substance sulfamethazine sulfate swine swine dysentery tablets tains tenella tion tissue treatment turing or feeding tylosin veterinarian weight gain weight per day Withdraw 5 days
Popular passages
Page 67 - ... concluded by such experts that the drug will have the effect it purports or is represented to have under the conditions of use prescribed, recommended, or suggested in the labeling or proposed labeling thereof.
Page 17 - If it is an imitation of another food, unless its label bears, in type of uniform size and prominence, the word "imitation" and, immediately thereafter, the name of the food imitated.
Page 38 - new drug" means — (1) Any drug (except a new animal drug or an animal feed bearing or containing a new animal drug) the composition of which is such that such drug is not generally recognized, among experts qualified by scientific training and experience to evaluate the safety and effectiveness of drugs, as safe and effective for use under the conditions prescribed, recommended, or suggested in the labeling thereof, except that such a drug not so recognized shall not be deemed to be a "new drug...
Page 551 - XIX Central Intelligence Agency (Parts 1900—1999) XX Information Security Oversight Office, National Archives and Records Administration (Parts 2000—2099) XXI National Security Council (Parts 2100—2199...
Page 78 - Secretary when the application was approved, shows that such drug is not shown to be safe for use under the conditions of use upon the basis of which the application was approved...
Page 38 - ... if at any time prior to the enactment of this Act it was subject to the Food and Drugs Act of June 30, 1906, as amended, and if at such time its labeling contained the same representations concerning the conditions of its use...
Page 22 - A food shall be exempt while held for sale from the requirements of section 403(k) of the act (requiring label statement of any artificial flavoring, artificial coloring, or chemical preservatives) if said food, having been received in bulk containers at a retail establishment, is displayed to the purchaser with either (1) the labeling of the bulk container plainly in view or (2) a counter card, sign, or other appropriate device bearing prominently and conspicuously the Information required to be...
Page 561 - Agency Defense Intelligence Agency Defense Logistics Agency Engineers, Corps of Federal Acquisition Regulation National Imagery and Mapping Agency Navy Department Secretary of Defense, Office of Defense Contract Audit Agency Defense Intelligence Agency Defense Logistics Agency Defense Nuclear Facilities Safety Board Delaware River Basin Commission...
Page 21 - The labeling of a food which contains two or more ingredients may be misleading by reason (among other reasons) of the designation of such food in such labeling by a name which includes or suggests the name of one or more but not all such ingredients, even though the names of all such ingredients are stated elsewhere in the labeling.
Page 78 - ... (B) that on the basis of new information before Kim, evaluated together with the evidence before him when the application was approved, the methods used in, or the facilities and controls used for, the manufacture, processing, and packing of...