The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 1978 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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1.–5. rezultāts no 100.
5. lappuse
... Products of Animals 500.80 Chemical compounds used in food- producing animals ; procedures and crite- ria for determining the acceptability of assay methods for carcinogenic residues in edible products of such animals . 500.84 Metabolic ...
... Products of Animals 500.80 Chemical compounds used in food- producing animals ; procedures and crite- ria for determining the acceptability of assay methods for carcinogenic residues in edible products of such animals . 500.84 Metabolic ...
7. lappuse
... products may occur through inadequate heat treatment of the product during its processing or through recontamination of the heat- treated product during a time of im- proper storage or handling subsequent to processing . ( b ) Articles ...
... products may occur through inadequate heat treatment of the product during its processing or through recontamination of the heat- treated product during a time of im- proper storage or handling subsequent to processing . ( b ) Articles ...
9. lappuse
... product preservative system for products used on non - food - producing animals at a level not exceeding 0.1 percent shall submit a new animal drug application , supplement an existing application , or reformulate the product by ...
... product preservative system for products used on non - food - producing animals at a level not exceeding 0.1 percent shall submit a new animal drug application , supplement an existing application , or reformulate the product by ...
10. lappuse
... product intended for use in or on animals implies that such product is capable of a therapeutic effect ( s ) and causes such a product to be a drug within the meaning of sec- tion 201 ( g ) of the Federal Food , Drug , and Cosmetic Act ...
... product intended for use in or on animals implies that such product is capable of a therapeutic effect ( s ) and causes such a product to be a drug within the meaning of sec- tion 201 ( g ) of the Federal Food , Drug , and Cosmetic Act ...
11. lappuse
... product intended for use in or on animals implies that such product is capable of a therapeutic effect ( s ) and causes such a product to be a drug within the meaning of sec- tion 201 ( g ) of the act . The unqualified use of such terms ...
... product intended for use in or on animals implies that such product is capable of a therapeutic effect ( s ) and causes such a product to be a drug within the meaning of sec- tion 201 ( g ) of the act . The unqualified use of such terms ...
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accordance acid administered amended at 42 Amount ampicillin Amprolium animal drug animal feed antibiotic application aqueous Arsanilic acid bacitracin bacterial body weight cattle chapter chloramphenicol chlortetracycline cloxacillin coccidiosis Conditions contains not less dihydrostreptomycin dosage forms dose erythromycin facturing or feeding Federal law restricts feed efficiency feeding practice feeds containing food additive Food and Drug g/ton grams hydrochloride immediate container Indications ingredient injection labeling licensed veterinarian Limitations manu ment milligrams milligrams per pound milliliters mycin neomycin novobiocin ointment oral oxytetracycline package paragraph percent phosphate polymyxin potassium pound of body premix prevention of coccidiosis procaine penicillin Proceed as directed Product promotion and feed recognized as safe Related tolerances Requirements for certification residues restricts this drug retort sample slaughter sodium sole source solution Specifications Sponsor Standards of identity sterile streptomycin submitted Subpart substance sulfate swine tablets tains tests and assays Tests and methods tetracycline tion treatment tylosin veterinarian
Populāri fragmenti
127. lappuse - ... a full list of the articles used as components of such drug; (3) a full statement of the composition of such drug; (4) a full description of the methods used in, and the facilities and controls used for, the manufacture, processing, and packing of such drug...
132. lappuse - Identity, strength, quality, and purity and were not made adequate within a reasonable time after receipt of written notice from the Secretary specifying the matter complained of; or (3) That on the basis of new information before him, evaluated together with the evidence before him when the application was approved, the labeling of such drug...
79. lappuse - 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...
132. lappuse - ... substantial evidence 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 proposed labeling thereof. . . . [T]he term "substantial evidence...
28. lappuse - Where the food is not manufactured by the person whose name appears on the label, the name shall be qualified by a phrase that reveals the connection such person has with such food; such as "Manufactured for ", "Distributed by ", or any other wording that expresses the facts.
79. lappuse - The composition of which is such that such drug, as a result of investigations to determine its safety and effectiveness for use under such conditions, has become so recognized but which has not, otherwise than in such investigations, been used to a material extent or for a material time under such conditions.
132. lappuse - New evidence not contained in such application or not available to the Secretary until after such application was approved, or tests by new methods, or tests by methods not deemed reasonably applicable when such application was approved, evaluated together with the evidence available to the Secretary when the application was approved...
31. lappuse - 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...
30. lappuse - Among representations in the labeling of a food which render such food misbranded is a false or misleading representation with respect to another food or a drug, device, or cosmetic. (b) 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...
36. lappuse - ... introduced such shipment or delivery into interstate commerce upon refusal by such person to make available for inspection a copy of the agreement, as required by paragraph (d) (2) or (3) of this section.