A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments, 24. sējumsU.S. Department of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, 1979 |
Citi izdevumi - Skatīt visu
Bieži izmantoti vārdi un frāzes
89th Congress act to amend amending the Federal AMENDMENTS OF 1967 ANIMAL DRUG AMENDMENTS animal feed bearing antibiotic application filed pursuant application was approved application with respect approving the application bacitracin basic Act basis batch bearing or containing bill to amend certification Chairman chloramphenicol chlortetracycline clause clearance Committee on Interstate Congress consignee Cosmetic Act Drug Administration drug application drug is intended drug is safe drug listed drug manufactured effect an approval effective date establish exemption Federal Food feed manufacturers food additive Food and Drug Foreign Commerce House ingredients inserting Interstate and Foreign investigations issue an order legislation methods opportunity for hearing paragraph penicillin prescribed procedure proposed labeling thereof public health purity purposes pursuant to subsection registrant regulations reports Rept safety and effectiveness Secretary finds section 512 standards of identity streptomycin suant submitted subparagraph tion United States Code United States Pharmacopeia Welfare
Populāri fragmenti
222. 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...
239. lappuse - That all charges for storage, cartage, and labor on goods which are refused admission or delivery shall be paid by the owner or consignee, and in default of such payment shall constitute a lien against any future importation made by such owner or consignee. SEC. 12. That the term "Territory" as used in this Act shall include the insular possessions of the United States. The word "person...
447. 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...
213. lappuse - A food shall be deemed to be adulterated— (a) (1) If it bears or contains any poisonous or deleterious substance which may render it injurious to health...
214. lappuse - That this paragraph shall not apply to any confectionery by reason of its containing less than one-half of 1 per centum by volume of alcohol derived solely from the use of flavoring extracts, or to any chewing gum by reason of its containing harmless nonnutritive masticatory substances.
470. lappuse - ... 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.
206. lappuse - CHANGES IN EXISTING LAW MADE BY THE BILL, As REPORTED In compliance with clause 3 of rule XIII of the Rules of the House of Representatives, changes in existing law made by the bill, as reported, are shown as follows (existing law proposed to be omitted is enclosed in black brackets, new matter is printed in italic, existing law in which no change is proposed is shown in roman...
223. lappuse - ... 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...
213. lappuse - ... 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...
450. lappuse - The alteration, mutilation, destruction, obliteration, or removal of the whole or any part of the labeling of, or the doing of any other act with respect to, a food, drug, device, or cosmetic, if such act is done while such article is held for sale (whether or not the first sale) after shipment in interstate commerce and results in such article being adulterated or misbranded.