17752. Adulteration and Misbranding of fluid extract of ergot, tincture cincbona compound, tincture nux vomica, tincture belladonna, fluid extract of belladonna leaves, and tincture cincbona. U. S. v. C. F. Sauer Co. Plea of guilty. Fine, S25. (F. & D. No. 25005. I. S. Nos. 03308, 03311, 04102, 04104, 04105, 04114.) Examination of samples of drugs from the herein-described interstate ship- ments having shown that the said samples did not conform to the United States Pharmacopoeia, the Secretary of Agriculture reported the matter to the United States attorney for the Eastern District of Virginia. On September 17, 1930, the said United States attorney filed in the District Court of the United States for the district aforesaid an information against the C. F. Sauer Co., a corporation, Richmond, Va., alleging shipment by said company under the name of the American Laboratories (Inc.), in violation of the food and drugs act, in various consignments, on or about July 25, August 21, October 26, and December 14, 1928, respectively, from the State of Virginia into the District of Columbia of quantities of fluid extract of ergot, tincture cinchona compound, tincture nux vomica, tincture belladonna, fluid extract of bella- donna leaves, and tincture cinchona, which were adulterated and misbranded. The articles were labeled in part: "Fluidextract Ergot (U. S. P.) ;" "Tinct. Cinchona, Comp. U. S. P.; " " Tinct. Nux Vomica U. S. P.;" " Tinct. Belladonna (U. S. P);" "Fluidextract Belladonna Leaves, U. S. P;" and "Tincture Cinchona, U. S. P." It was alleged in the information that the articles were adulterated in that they were sold under and by names recognized in the United States Pharma- copoeia and differed from the standard of strength, quality, and purity as deter- mined by the tests laid down in the said pharmacopoeia, viz: Thei said fluid extract of ergot was inert. The said tincture cinchona compound yielded not less than 0.640 gram of the alkaloids of cinchona per 100 cubic centimeters, whereas the said pharmacopoeia provides that compound tincture of cinchona should yield not more than 0.5 gram of the alkaloids of cinchona. The said tincture nux vomica yielded not less than 0.275 gram of the alkaloids of nux vomica per 100 cubic centimeters, whereas the pharmacopoeia provided that tincture of nux vomica should yield from each 100 cubic centimeters not more than 0.263 gram of the alkaloids of nux vomica. The said tincture belladonna yielded not less than 0.0463 gram of the alkaloids of belladonna leaves per 100 cubic centimeters, whereas the said pharmacopoeia provided that tincture of belladonna should yield from each 100 cubic centimeters not more than 0.033 gram of the alkaloids of belladonna leaves. The said fluid extract belladonna leaves yielded not less than 0.518 gram of the total alkaloids of belladonna leaves per 100 cubic centimeters, whereas the said pharmacopoeia provides that fluid extract belladonna leaves should yield from each 100 cubic centimeters not more than 0.33 gram of the total alkaloids of belladonna leaves. The said tincture cinchona yielded not more than 0.526 gram of the alkaloids of cinchona per 100 cubic centimeters, whereas the said pharmacopoeia provided that tincture cinchona should yield from each 100 cubic centimeters not less than 0.8 gram of the alkaloids of cinchona; and the standard of strength, quality, and purity of the said articles was not declared on the container thereof. Adulteration was alleged for the further reason that the strength and purity of the articles fell below the professed standard and quality under which they were sold in that they were represented to conform to the United States Pharmacopoeia, whereas they did not. Misbranding was alleged for the reason that the statements, "Fluidextract Ergot (U. S. P.)," "Tinct. Cinchona Comp. U. S. P.," "Tinct. Nux Vomica U. S. P.," "Tinct. Belladonna (U. S. P.)," "Fluidextract Belladonna Leaves U. S. P.," and " Tincture Cinchona U. S. P.," borne on the labels of the respec- tive articles, were false and misleading in that the said statements represented that the articles conformed to the standard laid down in the United States Pharmacopoeia, whereas they did not. On October 6, 1930, a plea of guilty to the information was entered on behalf of the defendant company, and the court imposed a fine of $25. ABTHTJB M. HYDE, Secretary of Agriculture.