8798. Misbranding of Vitamato. U. S. v. 1,046 Cases of Vitamato. Consent decree of condemnation. Product ordered released for relabeling. (F. D. C. No. 12439. Sample No. 29860-F.) LIBEL FILED : May 31, 1944, District of Hawaii. ALLEGED SHIPMENT: On or about May 1, 1944, by the Login Corporation, from San Francisco, Calif. PRODUCT: 1,046 cases, each containing 24 12-ounce bottles, of Vitamato at Honolulu, T. H. This product consisted of finely comminuted tomato material, diluted with water containing added dextrose, salt, and spices, and containing insignificant amounts of vitamins C and Bi. LABEL, IN PART : "Contains Vitamins A, B & C Enriched with Dextrose [vig- nette of a tomato] VITAMATO A Delicious Refreshing Cocktail Made From Tomatoes, Water, Dextrose, Salt, Citric Acid and Spices." NATURE OF CHARGE: Misbranding, Section 403 (a), the vignette of a tomato, the name "Vitamato," and the statements, "A Delicious Refreshing Cocktail Made From Tomatoes * * * Contains Vitamins * * * B & C," ap- pearing on the label, were false and misleading since the statements and design represented and suggested that the article was a tomato juice cocktail, a product generally understood to be tomato juice with added spices, with or without lemon juice, and that it contained nutritionally consequential amounts of vitamins Bi and C in the amounts normally present in tomato juice or tomato juice cocktail. The article was not tomato juice or tomato juice cocktail, and it contained substantially smaller amounts of vitamins Bi and C than are present in tomato juice or tomato juice cocktail. Further misbranding, Section 403 (a), the statement "Enriched with Dex- trose" suggested that the nutritional value of the article had been significantly improved by the addition of dextrose, whereas its nutritional value had not been significantly improved. DISPOSITION: July 1, 1944. Theo. H. Davies & Co., Ltd., Honolulu, T. H., claimant, having admitted that the labeling of the product was false and misleading, judgment of condemnation was entered and the product was ordered released for relabeling under the supervision of the Food and Drug Administration.