ViaDerma, Inc. announced that the Company has filed with the (FDA) Food and Drug Administration for a new over the counter or OTC version of its "Premature Ejaculation Drug". The new "OTC Drug" should have FDA registration approval in approximately 8 weeks and the Company's name of the new drug will portray prolonged endurance. The Company's recent testing of the drug has proved to be successful in retarding the onset of ejaculation during sexual intercourse.