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" That no drug defined in the United States 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... "
Annual Report of the Dairy and Food Commissioner of the State of Michigan - หน้า 187
โดย Michigan. Office of Dairy and Food Commissioner - 1909
มุมมองทั้งเล่ม - เกี่ยวกับหนังสือเล่มนี้

Acts Passed at the ... Session of the General Assembly for the Commonwealth ...

Kentucky - 1918 - 808 หน้า
...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 made by the test laid down in the United States Pharmacopoeia or National Formulary. Second. If the...

Biennial report of the Louisiana State Board of Health. 1906/07

1908 - 696 หน้า
...adulterated under this provision if the standard of strength, quality, or purity be plainly stated upon the bottle, box, or other container thereof although...from that determined by the test laid down in the Unites States Pharmacopoeia or National Formulary. Second. If its strength or purity fall below the...

The Tribune Almanac and Political Register

1907 - 396 หน้า
...provided that for the purposes of this act an article shall be v be adulterated: In case of drugs: tbntwe Second. If its strength or purity fall below the • professed standard or quality wlfr which it is sold. Jn the cape of confectionery: If И contains terra alba, baryte*, talc, chrome...

The Medical Brief: A Monthly Journal of Scientific Medicine and ..., เล่มที่ 38

1910 - 806 หน้า
...adulterated under this provision if the standard of strength, quality or purity be plainly stated upon the bottle, box or other container thereof, although...down in the United States Pharmacopoeia or National Formulary. If the Coudrey amendment is enacted according to his proposal, it will make this clause...

Public health reports (1881). v. 28 pt ..., เล่มที่ 28,ส่วนที่ 2,ฉบับที่ 27-52

1914 - 1550 หน้า
...adulterated under this provision if the standard of strength, quality, or purity be plainly stated upon y, or purity, as determined by the test laid down...at the time of investigation: Provided, That no dru Formulary." Sec. 739 (as amended). "That a flavoring extract is a solution iu ethyl alcohol of proper...

Meyer Brothers Druggist, เล่มที่ 36

1915 - 464 หน้า
...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...down in the United States Pharmacopoeia or National Formulary. Sec. 4. Food shall be deemed to be adulterated: * * * 9. If, in the case of confectionery,...

The Medical Fortnightly, เล่มที่ 29-30

1906 - 760 หน้า
...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 irom that determined by the test laid down in the United States Pharmacopeia . or National Formulary....

Hygienic Laboratory bulletin. no. 106-109, 1916-17, ฉบับที่ 106-109

1917 - 684 หน้า
...adulterated under this provision if the standard of strength, quality, or purity be plainly stated upon the bottle, box, or other container thereof, although...standard may differ from that determined by the test hud down in the United States Pharmacopoeia or in the National Formulary. During the decade that has...

Hygienic Laboratory bulletin. no. 41, 1908, ฉบับที่ 41

1908 - 842 หน้า
...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...

Transactions of the Kansas Academy of Science, เล่มที่ 20-21

Kansas Academy of Science - 1906 - 918 หน้า
...Pharmacopoeia or National Formulary, they differ from the standard of strength, purity or quality as determined by the test laid down in the United States Pharmacopoeia or National Formulary official at the time of investigation." Provision is made whereby these drugs may not be...




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