Food and Drug Administration's Food Labeling Regulation, Its Effect on Small Business: Hearings Before the Subcommittee on Special Small Business Problems of the Committee on Small Business, House of Representatives, Ninety-fifth Congress, Second Session, Washington, D.C., July 13, August 3, 1977, and March 15, 1978U.S. Government Printing Office, 1978 - 197 páginas |
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Página 2
... common " or usual name has been approved by FDA . Mr. Chairman , none of us in the baking industry can argue with the intent of this order , to disclose fully and completely the ingredients of our products . It is when one examines in ...
... common " or usual name has been approved by FDA . Mr. Chairman , none of us in the baking industry can argue with the intent of this order , to disclose fully and completely the ingredients of our products . It is when one examines in ...
Página 27
... common or usual names of those ingredients . However , a specific ingredient , unless it has become widely known in another way - by so - called " common or usual " name is often accurately identified only by its chemical name . An ...
... common or usual names of those ingredients . However , a specific ingredient , unless it has become widely known in another way - by so - called " common or usual " name is often accurately identified only by its chemical name . An ...
Página 51
... common or usual names for certain ingredients used by bakers . Mr. Quinn told the visitors that we would expedite their petition as soon as possible . Mr. Quinn did point out that it has been FDA's policy in the past to require that the ...
... common or usual names for certain ingredients used by bakers . Mr. Quinn told the visitors that we would expedite their petition as soon as possible . Mr. Quinn did point out that it has been FDA's policy in the past to require that the ...
Página 65
... common or usual names and mandatory / voluntary percentage of in- gredient labeling be adopted by the Food and Drug Administration in the follow- ing format : § 102.1a Common or usual names for nonstandardized foods . ( a ) The common or ...
... common or usual names and mandatory / voluntary percentage of in- gredient labeling be adopted by the Food and Drug Administration in the follow- ing format : § 102.1a Common or usual names for nonstandardized foods . ( a ) The common or ...
Página 66
... common or usual name of the ingredient or component . The word " containing " ( or " contains " ) , when used , shall appear on a line immediately below the name of the food in easily legible boldface print or type in distinct contrast ...
... common or usual name of the ingredient or component . The word " containing " ( or " contains " ) , when used , shall appear on a line immediately below the name of the food in easily legible boldface print or type in distinct contrast ...
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Términos y frases comunes
acid added addition advisory opinion amended ascorbic acid BOTTY bread breakfast cereals Bureau casein chapter Commis Commissioner advises Commissioner concludes Commissioner of Food common or usual CONGRESS THE LIBRARY consumer contain Cosmetic Act dietary diglycerides dough conditioners Drug Administration employees established exemption fat or oil fats and oils fats and/or oils Federal Food FEDERAL REGISTER final regulation finished food flour food additive Food and Drug food labeling gredient Hearing Clerk Independent Bakers ingredient labeling ingredient statement interested person issue juice label declaration LIBRARY OF CONGRESS manufacturers margarine matter meeting ment milk milligrams NAS/NRC Committee niacin notice nutrients nutritional nutritional quality guidelines optional ingredients order of predominance package paragraph percent petition plant protein product public hearing pursuant request Russo sioner sirup specific standard of identity submitted Subpart sumers sweeteners thiamine tion U.S. RDA usual name vitamin yeast
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Página 124 - ... agency action" includes the whole or a part of an agency rule, order, license, sanction, relief, or the equivalent or denial thereof, or failure to act; and (14) "ex parte communication" means an oral or written communication not on the public record with respect to which reasonable prior notice to all parties is not given, but it shall not include requests for status reports on any matter or proceeding covered by this subchapter.
Página 71 - The nutritional statements made in this advertisement have been reviewed by the Council on Foods and Nutrition of the American Medical Association and found consistent with current authoritative medical opinion.
Página 62 - ... the grounds for the objections. If a hearing is requested, the objections shall state the Issues for the hearing, shall be supported by grounds factually and legally sufficient to Justify the relief sought and •hall Include a detailed description and analysis of the factual Information Intended to be presented In support of the objections In the event that a hearing Is held.
Página 140 - ... because of its toxicity or other potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use...
Página 123 - Section 602 (b) of the act provides for the establishment by regulation of reasonable variations and exemptions for small packages from the required declaration of net quantity of contents. Section 5(b) of the Fair Packaging and Labeling Act provides for the establishment by regulation of exemptions from certain...
Página 133 - A person outside the executive branch may invite an agency representative to attend or participate in a meeting outside agency offices. The agency representative is not obligated to attend or participate, but may do so where it is in the public interest and will promote the objectives of the act.
Página 124 - advisory committee" means any committee, board, commission, council, conference, panel, task force, or other similar group, or any subcommittee or other subgroup thereof...
Página 101 - ... if it consists in whole or in part of any filthy, putrid, or decomposed substance, or if it is otherwise unfit for food; or (4) if it has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health...
Página 64 - Part 1 Regulations for the enforcement of the Federal Food, Drug, and Cosmetic Act and the Fair Packaging and Labeling Act.
Página 132 - ... require the party to show cause why his claim or interest in the proceeding should not be dismissed, denied, disregarded, or otherwise adversely affected on account of such violation...