 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...  The American Food Journal - Page 51907Full view - About this book
 | 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... | |
 | 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... | |
 | United States. Patent Office - 1912 - 662 pages
...time of investigation : Provided that, no drug denned in the United States Pharmacopoeia, or Rational Formulary, shall be deemed to be adulterated under...down in the United States Pharmacopoeia, or National Formulary. Second, if its strength or purity fall below the professed standard, or quality under which... | |
 | 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... | |
 | 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...States Pharmacopoeia or National Formulary." Sec. 739 (as amended). "That a flavoring extract is a solution iu ethyl alcohol of proper strength of the... | |
 | 1915 - 464 pages
...mixed or compound. Sec. 3. A drug shall be deemed to be adulterated within the meaning of this act: 1. If, when sold under or by a name recognized in the...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... | |
 | 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.... | |
 | 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... | |
 | 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... | |
 | 1904 - 1652 pages
...in the United States Pharmacopoeia official at the time of the investigation: Provided, That no drug shall be deemed to be adulterated under this provision...bottle, box, or other container thereof, although such standard may differ from that determined by the test laid down in the United States Pharmacopoeia.... | |
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