United States Congressional Serial SetU.S. Government Printing Office, 1909 Reports, Documents, and Journals of the U.S. Senate and House of Representatives. |
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หน้า 18 - First. If It be an imitation of or offered for sale under the distinctive name of another article. 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...
หน้า 522 - Report No. 2 on the origin and prevalence of typhoid fever in the District of Columbia, 1907.
หน้า 21 - Regulation 28 of the Rules and Regulations for the enforcement of the Food and Drugs Act was amended as follows: ". . . Acetanilide (antifebrine, phenylacetamide).
หน้า 20 - That the Secretary of the Treasury, the Secretary of Agriculture, and the Secretary of Commerce and Labor shall make uniform rules and regulations for carrying out the provisions of this Act...
หน้า 17 - 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...
หน้า 50 - New and Nonofficial Remedies. Since publication of New and Nonofficial Remedies, 1912, and in addition to those previously reported, the following articles have been accepted by the Council on Pharmacy and Chemistry of the American Medical Association for inclusion with "New and Nonofficial Remedies.
หน้า 521 - No. 32. — A stomach lesion in guinea pigs caused by diphtheria toxine and its bearing upon experimental gastric ulcer. By MJ Rosenau and John F. Anderson. No.
หน้า 521 - No. 21. — The immunity unit for standardizing diphtheria antitoxin (based on Ehrlich's normal serum). Official standard prepared under the act approved July 1, 1902. By MJ Rosenau. *No.
หน้า 17 - Pharmacopeia 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.
หน้า 511 - Vanilla extract is the flavoring extract prepared from vanilla bean, with or without one or more of the following: Sugar, dextrose, glycerin. It contains in 100 cubic centimeters the soluble matters from not less than 10 grams of the vanilla bean.