Abstract: An organoleptically acceptable antacid lozenge including at least one antacid present in the form of micronized particles having a particle size of less than about 10 microns. The lozenge is a solid oral composition capable of dissolving slowly in the mouth for long lasting administration of an antacid at a sustained or slow release rate. The lozenge is non-gritty, smooth textured, and does not irritate the oral mucosa.

Abstract: The present invention provides an organoleptically pleasing lozenge containing an antitussive selected from the group consisting of dextromethorphan, diphenhydramine, caramiphen, carbapentane, ethylmorphine, noscapine, codeine, and mixtures thereof, complexed with an ion exchange resin wherein the particle size of the resin is 38 ?m or less in diameter. Also provided is a process for producing the lozenge and methods of administering the lozenge.

Abstract: A pleasant-tasting, substantially alcohol-free oral mouthwash composition is effective in eliminating the bacteria and other oral microflora responsible for the production of plaque, periodontitis, gingivitis, gum disease and bad breath. The composition consists of a unique blend of the essential oils thymol or eucalyptol, methyl salicylate, menthol and tripartite blend of peppermint flavor oils that are dissolved in solution using a non-ionic surfactant blend.

Abstract: The invention provides a dissolution cell and method for determining the in-vitro release rate of a drug in suitable form, e.g. a suppository. The cell includes a solid rectangular top wall and a pair of trapezoidal side walls extending from the top wall. Disposed between the side walls are a pair of end walls and a bottom wall each comprised of a wire mesh material. The bottom wall and end walls can be made in one piece. The top wall has an opening and a flanged extension which can be coupled to a suitable rotating device. In use the cell containing the drug is rotated in a suitable dissolution medium and the rate of release of the drug is determined by analyzing the amount of drug released to the dissolution medium at predetermined intervals.