8980. Adulteration and misbranding of vanilla extract. "U. S. v. 11 Dozen Bot- tles of Vanilla Extract. Default decree of condemnation; product or- dered delivered to Food and Drug Administration for technical purposes. (F. D. C. No. 3894. Sample No. 46731-E.)" This product was deficient in vanilla resins and contained artificial flavor and other substances foreign to vanilla extract as indicated by the presence of exces- sive mineral matter. On February 28,1941, the United States attorney for the District of New Jersey filed a libel against ll dozen bottles of vanilla extract at Hoboken, N. J., alleging that the article had been shipped by General Desserts Corporation from New York, N. Y., on or about December 19,1940; and charging that it was adulterated and misbranded. It was labeled in part: (Bottles) "Contents 4 Fl. Oz. * * * American House Pure Extract Vanilla." The article was alleged to be adulterated (1) in that an imitation vanilla extract deficient in vanilla resin and containing added ash material and artificial flavor had been substituted wholly or in part for "Pure Extract Vanilla"; (2) in that inferiority had been concealed through the addition of ash material and artificial flavoring; and (3) in that ash material and artificial flavoring had been added thereto or mixed or packed therewith so as to make it appear better or of greater value than it was. It was alleged to be misbranded (1) in that the statement "Pure Extract Vanilla" was false and misleading as applied to an imitation vanilla extract defi- cient in vanilla resin and containing added ash material and artificial flavoring; (2) in that it was offered for sale under the name of another food; (3) in that it was an imitation of another food and its label did not bear, in type of uniform size and prominence, the word "imitation" and, immediately thereafter, the name of the food imitated; and (4) in that it contained artificial flavoring and failed to bear labeling stating that fact. On September 4,1941, no claimant having appeared, judgment of condemnation was entered and the product was ordered delivered to the Food and Drug Admin- istration to be used for technical purposes.