Meyer Brothers Druggist, 27권,11호

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C.F.G. Meyer, 1906

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353 페이지 - Act, or is otherwise dangerous to the health of the people of the United States, or is of a kind forbidden entry Into, or forbidden to be sold or restricted in sale In the country In which it is made or from which It Is exported...
351 페이지 - 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...
352 페이지 - A reasonable variation from the stated weight for individual packages is permissible, provided this variation is as often above as below the weight or volume stated. This variation shall be determined by the inspector from the changes in the humidity of the atmosphere from the exposure of the package to evaporation or to absorption of water, and the reasonable variations which attend the filling and weighing or measuring of a package. Regulation 30.— Method of Stating Quantity or Proportion. {...
350 페이지 - The use of any false or misleading statement, design, or device shall not be justified by any statement given as the opinion of an expert or other person, appearing on any part of the label, nor by any descriptive matter explaining the use of the false or misleading statement, design, or device.
348 페이지 - An act for preventing the manufacture, sale, or transportation of adulterated or misbranded or poisonous or deleterious foods, drugs, medicines, and Hquors. and for regulating traffic therein, and for other purposes...
350 페이지 - Descriptive matter upon the label shall be free from any statement, design, or device regarding the article or the ingredients or substances contained therein, or quality thereof, or place of origin, which is false or misleading in any particular.
349 페이지 - A drug bearing a name recognized in the United States Pharmacopoeia or National Formulary, without any further statement respecting its character, shall be required to conform in strength, quality and purity to the standards prescribed or indicated for a drug of the same name recognized in the United States Pharmacopoeia or National Formulary official at the time.
350 페이지 - Foods." (a) The Secretary of Agriculture, when he deems it necessary, shall examine the raw materials used in the manufacture of food and drug products, and determine whether any filthy, decomposed, or putrid substance is used in their preparation. (b) The Secretary of Agriculture shall make such inspections as often as he may deem necessary. MISBRANDINC. REGULATION 17. LABEL. (Section 8.) (a) The term "label...
351 페이지 - Provided, That the term blend as used herein shall be construed to mean a mixture of like substances, not excluding harmless coloring or flavoring ingredients used for the purpose of coloring and flavoring only...
348 페이지 - Samples may be purchased in the open market, and if in bulk the marks, brands, or tags upon the package, carton, container, wrapper, or accompanying printed or written matter shall be noted. The collector shall also note the names of the vendor and agent through whom the sale was actually made, together with the date of purchase.

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