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" 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... "
The Food and Drugs Act, June 30, 1906: A Study with Text of the Act ... - Page 76
by Arthur Philip Greeley - 1907 - 176 pages
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Acts Passed at the ... Session of the General Assembly for the Commonwealth ...

Kentucky - 1918 - 808 pages
...down in the United States Pharmacopoeia' or National Formulary official at the time of investigation. Provided, that no drug defined in the United States...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...
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Biennial report of the Louisiana State Board of Health. 1906/07

1908 - 696 pages
...down in the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States...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...
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The Tribune Almanac and Political Register

1907 - 404 pages
...defined in the United Stales Pharmacopoeia or National Formulary shall be deemed to be adulterated thix provision if the standard of strength, quality or purity be plainly stated Ihfe bottle, box "or other container thereof, although the ertandard may differ from bat determined...
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The Medical Brief: A Monthly Journal of Scientific Medicine and ..., Volume 38

1910 - 806 pages
...down by the United States Pharmacopoeia or National Formulary official at the time of investigation ; Provided, That no drug defined in the United States...down in the United States Pharmacopoeia or National Formulary. If the Coudrey amendment is enacted according to his proposal, it will make this clause...
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Public health reports (1881). v. 28 pt. 2 ..., Volume 28, Part 2, Issues 27-52

1914 - 1550 pages
...down by the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States...down in the United States Pharmacopoeia or National Formulary." Sec. 739 (as amended). "That a flavoring extract is a solution iu ethyl alcohol of proper...
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Meyer Brothers Druggist, Volume 36

1915 - 464 pages
...therein. 2. If its strength, quality or purity fall below the professed standard under which it is sold: Provided, that no drug defined in the United States...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...
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The Medical Fortnightly, Volumes 29-30

1906 - 760 pages
...official at the time of investigation; Provided, That no drug defined in the United States Pharmacopeia or National Formulary shall be deemed to be adulterated...container thereof, although the standard may differ irom that determined by the test laid down in the United States Pharmacopeia . or National Formulary....
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Hygienic Laboratory bulletin. no. 106-109, 1916-17, Issues 106-109

1917 - 684 pages
...down in the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States...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...
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Hygienic Laboratory bulletin. no. 41, 1908, Issue 41

1908 - 842 pages
...official at the time of investigation : Provided. That no drug defined in the United States Pharmacopeia or National Formulary shall be deemed to be adulterated...of strength, quality, or purity be plainly stated u|K>n the bottle, hox, or other container thereof although the standard may differ from that determined...
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Transactions of the Kansas Academy of Science, Volumes 20-21

Kansas Academy of Science - 1906 - 918 pages
...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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