Bulletin - Bureau of Chemistry, Utgaver 100-109 |
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Bulletin - Bureau of Chemistry, Utgaver 125-134 United States. Bureau of Chemistry Uten tilgangsbegrensning - 1909 |
Bulletin - Bureau of Chemistry, Utgaver 1-12 United States. Bureau of Chemistry Uten tilgangsbegrensning - 1883 |
Bulletin - Bureau of Chemistry, Utgaver 142-154 United States. Bureau of Chemistry Uten tilgangsbegrensning - 1911 |
Vanlige uttrykk og setninger
adulteration Agriculture aliquot alkali ammonium hydroxid amount analysis barium beaker boiling bottle Bureau of Chemistry calcium carbon cc of water cent alcohol Chem chemical chemists chlorid coloring matter containing cool copper cottonseed meal cubic centimeters Dairy and Food Detection determination dilute dioxid dish dissolve distillate ether evaporate examination excess Expt extract fertilizer filter filtrate flask flour Food Comm gluten grams heat hydrochloric acid ignite insoluble iodin lead lime liquid meal meat method milk minutes mixture moisture neutral nitric acid nitrogen obtained oxid percentage phosphate phosphoric acid portion potash potassium pounds precipitate prepared present protein pure quantity reagents reducing sugars referee Rept residue salicylic acid sample shake sirup soda sodium hydroxid soluble solution specific gravity standard starch substances sucrose sulphate sulphid sulphuric acid Table tannin temperature tenth-normal tion titrate tube wash water bath weigh wine zinc
Populære avsnitt
Side 8 - misbranded," as used herein, shall apply to all drugs, or articles of food, or articles which enter into the composition of food, the package or label of which shall bear any statement, design, or device regarding such article, or the ingredients or substances contained therein which shall be false or misleading in any particular...
Side 8 - 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...
Side 7 - Second. If any substance has been substituted wholly or in part for the article. Third. If any valuable constituent of the article has been wholly or in part abstracted. Fourth. If it be mixed, colored, powdered, coated, or stained in a manner whereby damage or inferiority is concealed.
Side 8 - 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," or "blend," as the case may be, is plainly stated on the package in which it is offered for sale: Provided, That the term, blend...
Side 7 - drug" as used in this act, shall include all medicines and preparations recognized in the United States Pharmacopoeia or National Formulary for internal or external use, and any substance or mixture of substances intended to be used for the cure, mitigation, or prevention of disease of either man or other animals. The term "food...
Side 10 - 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 corporation, company, society, or association, within the scope of his employment or office, shall in every case be also deemed to be the act, omission,, or failure of such corporation, company, society, or association as well as that of the person.
Side 7 - ... 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 шау differ from that determined by the test laid down in the United States Pharmacopoeia or National Formulary.
Side 43 - In the case of food, drink, flavoring extract, confectionery or condiment : (1) If any substance or substances have been mixed with it. so as to lower or depreciate, or injuriously affect its quality, strength or purity ; (2) If any inferior or cheaper substance or substances have been substituted wholly or In part for it; (3) if any valuable or necessary constituent or ingredient has been wholly or in part abstracted from it...
Side 7 - First. If, when a drug is sold under or by a name recognized in the United States Pharmacopoeia or National Formulary, it differs from the standard of strength, quality, or purity, as determined by the test laid down in the United States Pharmacopoeia or National Formulary official at the time of investigation : Provided, That no drug defined in the United States Pharmacopoeia or National Formulary...
Side 9 - That upon the payment of the costs of such libel proceedings and the execution and delivery of a good and sufficient bond to the effect that such articles shall not be sold or otherwise disposed of contrary to the provisions of this Act or the laws of any State, Territory, or District, the court may by order direct that such articles be delivered to the owner thereof.