924. Adulteration and misbranding of Azamine Capsules. IT. S. v. 4 Boxes of Azamlne Capsules. Default decree of condemnation. Product ordered destroyed. (F. D. C. No. 8018. Sample No. 7216-F.) This product contained the active ingredient in excess of the amount declared on the label, and it would not be an effective treatment for various disease con- ditions for which it was recommended in the labeling. On July 31, 1942, the United States attorney for the Eastern District of Wis- consin filed a libel at Milwaukee, Wis., against 4 boxes of Azamine Capsules, alleging that the article had been shipped in interstate commerce on or about June 8, 1942, by the Nepera Chemical Co., Inc., from Tonkers, N. Y. Analysis of a sample of the article showed that each capsule contained not less than 5.89 grams (90.9 grains) of tolyl azo diamino pyridine hydrochloride. It was alleged to be adulterated in that its strength differed from that which it purported and was represented to possess. It was alleged to be misbranded in that the statement "5 Grams * * * Each capsule contains 5 grams (77.2 grs. app.) of Tolyl-Azo-Diamino-Pyridine- Hydrochloride," borne on the label, was false and misleading. The article was also alleged to be misbranded in that statements made in the labeling which represented and suggested that it was effective in the treatment of various disease conditions were false and misleading since it was not effective for these conditions. Some of the representations made were that Azamine has been shown to possess marked bactericidal power in coccal and B. coli infections, and that it was an antiseptic of proved value in a wide range of infections in large and small animals. It was recommended for mastitis, metritis, vesicular vaginitis, urinary infections, necrotic lesions, sinuses and fistulae, as well as for acute septic metritis, cystitis, nephritis, coccidiosis, gas- tritis, enteritis, septicemia and pyemia. It was also recommended as a topical application for udder and teat injuries, keratitis, conjunctivitis, and traumata of eye and associated tissues. On October 1, 1942, no claimant having appeared, judgment of condemnation was entered and the product was ordered destroyed.