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Foods and Their Adulteration: Origin, Manufacture, and Composition of Food ...
Harvey Washington Wiley
Uten tilgangsbegrensning - 1907
acid added addition adulteration Agriculture alcohol amount animal appearance applied artificial average become beef bodies butter cane carcasses character cheese chemical color common composition consumer contains corn Department drug edible eggs employed especially establishment extent extract fact fermentation fish flavor flesh flour food products fresh fruit give given glucose grown grows heat highly important indicated inspection juice kind known label lard less manufacture material matter means meat mentioned method milk mixed mushrooms natural obtained origin package percent plant portion potato pounds practically preparation present preserved principal proper properties protein quantity reason regarded regulations removed rendered respect salt samples Secretary secured seed separated sirup solid sometimes starch subjected substance sugar sweet temperature term United usually varieties vegetable weight wine
Side 523 - Pharmacopeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States Pharmacopoeia or National Formulary shall be deemed to be adulterated under this provision if the standard of strength, quality, or purity be plainly stated upon the bottle, box, or other container thereof although the standard may differ from that determined by the test laid down in the United States Pharmacopoeia or National Formulary.
Side 593 - Second. If it be labeled or branded so as to deceive or mislead the purchaser, or purport to be a foreign product when not so, or if the contents of the package as originally put up shall have been removed in whole or in part and other contents shall have been placed in such package, or if...
Side 525 - Act, the same shall be disposed of by destruction or sale, as the said court may direct, and the proceeds thereof, if sold, less the legal costs and charges, shall be paid into the Treasury of the United States, but such goods shall not be sold in any jurisdiction contrary to the provisions of this Act or the laws of that jurisdiction: Provided, however. That upon the payment of the costs of such libel proceedings and the execution and delivery of a good and sufficient bond...
Side 522 - District of Columbia, or foreign country, and having so received, shall deliver, in original unbroken packages, for pay or otherwise, or offer to deliver to any other person any such article so adulterated or misbranded within the meaning of this Act, or any person who shall sell or offer for sale in the District of Columbia or the Territories of the United States...
Side 525 - 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 584 - Second. In the case of articles labeled, branded, or tagged so as to plainly indicate that they are compounds, imitations, or blends, and the word "compound," "imitation,
Side 525 - ... for any cause to the custody of the Secretary of the Treasury, when demanded, for the purpose of excluding...
Side 522 - Labor shall make uniform rules and regulations for carrying out the provisions of this Act, including the collection and examination of specimens of foods and drugs manufactured or offered for sale in the District of Columbia, or in any Territory of the United States...
Side 521 - That the introduction into any State or Territory or the District of Columbia from any other State or Territory or the District of Columbia, or from any foreign country, or shipment to any foreign country of any article of food or drugs which is adulterated or misbranded, within the meaning of this Act...
Side 523 - Formulary shall be deemed to be adulterated under this provision if the standard of strength, quality, or purity be plainly stated upon the bottle, box, or other container thereof although the standard may differ from that determined by the test laid down in the United States Pharmacopeia and National Formulary. Second. If its strength or purity fall below the professed standard or quality under which it is sold.