A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments, Volum 3U.S. Department of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, 1979 |
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Side 6
... regulations as provided by 4 sections 303 , 701 , and 703 . 5 ( d ) If its labeling is false or misleading in any 6 particular . 7 ( e ) If in package form it fails to bear a label contain- 8 ing : ( 1 ) The name and place of business ...
... regulations as provided by 4 sections 303 , 701 , and 703 . 5 ( d ) If its labeling is false or misleading in any 6 particular . 7 ( e ) If in package form it fails to bear a label contain- 8 ing : ( 1 ) The name and place of business ...
Side 7
... regulations as provided by sections 303 , 701 , and 703 , and ( 1 ) its label fails to bear a statement of its quality in such terms as the regulations specify , or ( 2 ) its quality falls below such standard . 10 11 12 13 ( i ) If it ...
... regulations as provided by sections 303 , 701 , and 703 , and ( 1 ) its label fails to bear a statement of its quality in such terms as the regulations specify , or ( 2 ) its quality falls below such standard . 10 11 12 13 ( i ) If it ...
Side 10
... regulations prescribe 18 and to make regulations governing the issuance and renewal 19 thereof . The Secretary is authorized to suspend immedi- 20 ately upon notice any permit issued under authority of this 21 section if it is found ...
... regulations prescribe 18 and to make regulations governing the issuance and renewal 19 thereof . The Secretary is authorized to suspend immedi- 20 ately upon notice any permit issued under authority of this 21 section if it is found ...
Side 17
... regulations as provided by sections 701 18 and 703 : Provided , That no drug shall be deemed to be misbranded under this paragraph by reason of failure of 20 its labeling to bear a statement of any advertised use such advertising is ...
... regulations as provided by sections 701 18 and 703 : Provided , That no drug shall be deemed to be misbranded under this paragraph by reason of failure of 20 its labeling to bear a statement of any advertised use such advertising is ...
Side 21
... REGULATIONS & 14 SECTION 701. ( a ) The authority to make regulations for the efficient enforcement of this Act , except as otherwise is provided in this section , is hereby vested in the Secretary . ( b ) The Secretary of the Treasury ...
... REGULATIONS & 14 SECTION 701. ( a ) The authority to make regulations for the efficient enforcement of this Act , except as otherwise is provided in this section , is hereby vested in the Secretary . ( b ) The Secretary of the Treasury ...
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A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its ... Uten tilgangsbegrensning - 1979 |
A Legislative History of the Federal Food, Drug, and Cosmetic Act ..., Volum 1 United States Uten tilgangsbegrensning - 1979 |
A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its ... Uten tilgangsbegrensning - 1979 |
Vanlige uttrykk og setninger
adulterated or misbranded amendment was agreed antiseptic Association bill Chairman coal-tar colors committee Congress consignee consumer cosmetics court dangerous to health deemed definition and standard deleterious substance disease dissemination District Drug Administration Drugs Act effect enforcement establishment eucaine exemptions fact fails to bear false advertising Federal Food Federal Trade Commission flavors Food and Drug germicidal hearing industry ingredients injunction insert inspection interstate commerce jurisdiction KALLET label fails legislation libel manufacturer medicines ment methods metics package paragraph permit person poisonous or deleterious prescribed present law President PRESIDENT pro tempore proceedings prosecution protection provided by sections public health purposes reason regulations as provided represented Secretary is hereby Secretary of Agriculture sections 701 seizure Senator CLARK Senator COPELAND Senator GIBSON shipment soap sold standard of identity standard of quality statement sumer term thereof tion United States attorney United States Pharmacopoeia violation word
Populære avsnitt
Side 483 - The proceedings of such libel cases shall conform, as near as may be, to the proceedings in admiralty, except that either party may demand trial by jury of any issue of fact joined in any such case, and all such proceedings shall be at the suit of and in the name of the United States.
Side 653 - If any substance has been mixed or packed with it so as to reduce or lower or injuriously affect its quality or strength.
Side 303 - Act, it shall issue and serve upon such person a complaint stating its charges in that respect, and containing a notice of a hearing upon a day and at a place therein fixed at least thirty days after the service of said complaint. The person so complained of shall have the right to appear at the place and time so fixed and show cause...
Side 308 - Any person, firm, corporation, or association who, with intent to sell or in any wise dispose of merchandise, securities, service, or anything offered by such person, firm, corporation, or association, directly or indirectly, to the public for sale or distribution, or with intent to increase the consumption thereof, or to induce the public in any manner to enter into any obligation relating thereto, or to acquire title thereto...
Side 483 - And if such article is condemned as being adulterated or misbranded, or of a poisonous or deleterious character, within the meaning of this Act, the same shall be disposed of by destruction or sale, as the said court may direct...
Side 485 - When construing and enforcing the provisions of this Act, the act, omission, or failure of any officer, agent, or other person acting for or employed by any...
Side 689 - Act (1) small open containers of fresh fruits and fresh vegetables and (2) food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such food is not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, or repacking establishment.
Side 190 - ... an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count: Provided, That under clause (2) of this paragraph reasonable variations shall be permitted, and exemptions as to small packages shall be estab-lished, by regulations prescribed by the Secretary.
Side 192 - First. If, when a drug is sold under or by a name recognized in the United States Pharmacopreia or National Formulary, it differs from the standard of strength, quality, or purity, as determined by the test laid down in the United States Pharmacopeia or National Formulary official at the time of investigation...
Side 202 - ... brought into compliance with the provisions of this Act under the supervision of an officer or employee duly designated by the Secretary, and the expenses of such supervision shall be paid by the person obtaining release of the article under bond.