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    ASPARTAME
    July 26, 1974 - United States

    Aspartame artificial sweetener was approved by the U.S. Food and Drug Administration. Objections were raised about its safety, and the FDA issued a stay on 5 Dec 1975 after which followed several more years of tests, studies and scrutiny. Finally, it was approved on 22 Oct 1981 for permitted uses that included in candy, tablets, breakfast cereals, instant coffee and tea, gelatines, and chewing gum, among others. Years earlier, in Dec 1965, while working on an ulcer drug, James M. Schlatter had made the discovery that a mixture of two amino acids, aspartic acid and phenylalamine, had a sweet taste. By weight it was about 200 times sweeter than sugar, with very few calories. G.D. Seale marketed it as NutraSweet, a low-calorie artificial sweetener without the bitter aftertaste of saccharin.

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To provide outstanding medical and aesthetic dermatology to people of all ages. We are committed to rendering effective, confidential and respectful care to all of our patients, in a warm and pleasant environment. We pride ourselves on innovative thinking, constantly striving for advanced education and utilization of the latest technology to achieve the best possible results. Additionally, as a clinical research study site, we carefully evaluate every technology and procedure for safety and efficacy before offering these services to our patients. We employ a team of highly-trained, dedicated health care professionals who work together to provide consistent care throughout the practice. Patient satisfaction is key to the success of our practice. Aesthetic Solutions’ ultimate goal is to provide high-quality services and to form a relationship with our patients that is based on mutual trust and respect.

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