Abstract: A percutaneous preparation of tulobuterol is disclosed, comprising a support having thereon a base layer comprising a pressure-sensitive adhesive containing tulobuterol, the pressure-sensitive adhesive comprising polyisobutylene. The preparation achieves persistent and effective administration of tulobuterol through the skin into the body.
Abstract: The present invention is a method and a dosage unit for delivery of a controlled-release system. The dosage unit is a quick dissolve unit which can be prepared by mixing uncured shearform matrix and a controlled-release system, either molding or compacting a unit dosage form and curing the shearform matrix. The controlled-release systems used in the present invention include instantaneous release components, delayed release components, sustained release components, and combinations thereof.
Type:
Grant
Filed:
November 4, 1994
Date of Patent:
October 22, 1996
Assignee:
Fuisz Technologies Ltd.
Inventors:
Garry L. Myers, Gerald E. Battist, Richard C. Fuisz
Abstract: An improved liquid skin cleanser composition will have about 0.1-25% by weight of at least one EO/PO/EO tri-block nonionic surfactant having the formula: ##STR1## wherein neither x or z can be 0; the sum of x and z is within the range of about 62 to 535, the value of y is within the range of about 15 to 65. Also present will be about 0.1-25% by weight polyvinylpyrrolidone having the formula: ##STR2## wherein the value of n ranges from about 100 to 30,000.
Abstract: The present invention refers to the use of 5-methyltetrahydrofolic acid, of 5-formyltetrahydrofolic acid and of their pharmaceutically acceptable salts for the preparation of controlled release pharmaceutical compositions suitable for the use in the therapy of depressive disturbances, in particular major depression, dysthymia or depressive neurosis and not otherwise specified depressive disturbances, independently from folate plasmatic levels, and to the pharmaceutical composition thus prepared.
Abstract: A mascara composition containing at least one curl retention additive to help enhance and sustain a curl along with a hair fixative resin designed to hold the eyelashes in a curled position by preventing the fixed eyelash hairs from being affected by humidity.
Abstract: Water-soluble borate-polyol complexes are useful as buffers and/or antimicrobials in aqueous ophthalmic compositions, including those containing polyvinyl alcohol. These compositions have greater antimicrobial activity than comparable compositions containing typical borate buffers and unexpectedly increase the antimicrobial efficacy of other antimicrobial agents when used in combination. In addition, use of the borate-polyol complexes avoids the incompatibility problem typically associated with the combination of borate buffer and polyvinyl alcohol; therefore, the compositions disclosed herein may also contain polyvinyl alcohol.
Abstract: A barrier film comprising a flexible substantially of transparent substrate having first and second surfaces. A substantially colorless barrier coating is formed on at least one of said surfaces of a graphite material having a thickness ranging from 50 to 350 .ANG..
Type:
Grant
Filed:
April 26, 1994
Date of Patent:
March 19, 1996
Assignee:
Flex Products, Inc.
Inventors:
Roger W. Phillips, Paul G. Coombs, Lauren R. Wendt
Abstract: Chronic inflammatory intestinal diseases may be treated enterally pharmacologically active doses of said oxypurinol and or its alkali, alkaline earth, or ammonium salts.
Type:
Grant
Filed:
December 15, 1993
Date of Patent:
January 16, 1996
Assignee:
Henning Berlin GmbH Chemie-und Pharmawerk
Inventors:
Ekkehard Scheiffele, Gerhard Gerber, Werner Siems, Andreas Werner
Abstract: A novel process for the preparation of pharmaceutical compositions involving the stabilization of the active drug(s) through the reduction of residual alcohol present in a drug/carrier blend. The presence of residual alcohol in dried pharmaceutical compositions adversely affects many drugs which must be initially dissolved therein in order to achieve uniform distributions throughout the excipient carrier materials. Wherein not previously possible, its removal is achieved utilizing precise processing parameters in which water lost during the drying process is replenished during blending in a conventional solids processor.
Type:
Grant
Filed:
January 17, 1995
Date of Patent:
December 26, 1995
Assignee:
Warner-Lambert Company
Inventors:
Pankaj B. Gala, Gary D'Alonzo, Jatin J. Shah, Jay Weiss
Abstract: This invention is directed to a multilayered controlled release pharmaceutical dosage form. More particularly the dosage form is adapted for water soluble drugs and comprises a plurality of coated particles wherein each has multiple layers about a core containing a drug active whereby the drug containing core and at least one other layer of drug active is overcoated with a controlled release barrier layer and preferably an outer layer of additional drug is adapted for immediate release to preferably provide one immediate releasing layer and at least two controlled releasing layers of a water soluble drug from the multilayered coated particle.
Abstract: Patent of invention "process for obtaining an hair conditioner," comprising a process for obtaining an hair conditioner which imparts gloss, softness and elasticity to the hair and augments its tendency to maintain the desired shape of the hairdo; the active ingredients of the conditioner being ascorbic acid and cupric and/or cuprous salts: the conditioner in one version being presented in powder form, containing besides the active ingredients, thickening agents, being mixed with water before use and in another version presented in form of a cream, gel or paste, to be used on hair, in both cases containing, optionally, other ingredients of specific action.
Abstract: There is disclosed a synergistic composition and process for skin depigmentation with reduced irritation which does not employ a corticosteroid and which employs a substituted oxybenzene and a retinoid.
Abstract: Striae distensae lesions may be prevented and/or reduced in size by topically applying to the skin affected with the lesions an effective amount of a retinoid, preferably retinoic acid, preferably by daily application in a dermatologically acceptable vehicle, such as a cream base, at a concentration of about 0.025 to 0.1 weight percent retinoic acid. When applied during the striae rubrae stage, the retinoid may be effective to prevent the formation of striae albae lesions, and when applied in either stage, the retinoid may be effective to reduce the width and depth of the lesions, with improved texture and softness.
Abstract: Body powder is provided having microcapsules with a colorant located in or on the shell of said microcapsule. The microcapsules are present in an amount effective to impart color to the body powder when viewed in bulk and to substantially decrease in perceptible color upon rubbing said body powder on the skin.
Type:
Grant
Filed:
October 29, 1993
Date of Patent:
October 24, 1995
Assignee:
Minnesota Mining and Manufacturing Company
Inventors:
Robert A. Davis, Sheila M. Nichols, Howard J. Buttery
Abstract: A directly compressed cholestyramine tablet with a solvent-free coating is disclosed. The inner core of the tablet is made up of cholestyramine agglomerates consisting of numerous small, irregularly-shaped, jagged-edged fragments having relatively few smooth or flat surfaces with a moisture content ranging from about 8 to 14 percent by weight. A process is also disclosed for preparing cholestyramine agglomerates of the invention. The solvent-free coating comprises from about 60 percent to about 95 percent by weight of stearic acid and from about 5 percent to about 40 percent of polyethylene glycol.
Type:
Grant
Filed:
June 15, 1994
Date of Patent:
October 3, 1995
Assignee:
Bristol-Myers Squibb Company
Inventors:
Robert J. Bequette, Bruce A. Bonenberger, Claude E. Gallian, John R. Reckelhoff
Abstract: This invention provides an immunoenhancement or immunepotentiation therapy comprising administration of potassium, insulin, glucose and, optionally, thyroid, a cholinergic agent and bicarbonate. Therapeutic compositions comprising the above components in appropriate dosages are also provided.
Abstract: Pharmaceuticals formulations are described, in form of capsules ad oral use, containing as the active ingredient ubidecarenone, characterized in that the active ingredient is dispersed in a mixture of isopropyl myristate or isopropyl palmitate with polyethoxylated, hydrogenated or non hydrogenated, castor oils.
Abstract: There is disclosed: an absorbent, non-adherent, freeze-dried, fibre-free pad comprising from 2 to 6 parts by weight of a water-soluble biocompatible polymer and from 2 to 15 parts by weight of a liquid humectant, provided that the weight ratio of humectant to polymer is from 0.75:1 to 2.5:1 and; a method for producing the pad.
Abstract: A pharmaceutical composition for the prevention of sexually transmitted diseases, intended to be contacted with a mucosa. The composition contains, on the one hand, at least one constituent active against the viruses and bacteria responsible for the said sexually transmitted diseases and, on the other hand, a product inhibiting the penetration of the active constituent across a mucosa, in combination with a pharmaceutically acceptable vehicle adapted to the topical administration of this composition. Advantageously, the product inhibiting penetration is a film-former capable of forming a film with which the active constituent or constituents are associated.
Type:
Grant
Filed:
December 22, 1992
Date of Patent:
August 8, 1995
Assignee:
S S P L Safe Sex Products Licensing Societe Anonyme
Abstract: A skin cleansing and exfoliant composition comprising d-alpha tocopheryl acetate (Vitamin E) homogenized in a pharmacologically acceptable oil phase and an emulsion or suspension of retinoic acid or a pharmacologically acceptable derivative thereof in a pharmacologically acceptable fluid adapted for application to human or non-human animal skin, the portion of oil phase being sufficient to provide a concentration of oil phase in the emulsion or suspension of from about 20% to about 40% by weight and the portion of retinoic acid or derivative thereof being sufficient to provide a concentration in the emulsion or suspension of from about 60% to about 80% by weight. A method for using the composition is also disclosed.