Lexaryn Provides Herbal Alternative for Treating Erectile Dysfunction (ED)
A natural herbal pill -- Lexaryn (http://www.Lexaryn.com) – has been developed for men who experience erectile dysfunction (ED) and who are looking for an effective alternative to using prescription drugs. Manufactured under FDA guidelines, it is made using a proprietary formula of herbal ingredients.
“We designed Lexaryn to provide a natural alternative to the prescription drugs which are commonly prescribed to treat erectile dysfunction,” says Nathan Farkon, CEO of Lexaryn.com. “We developed the formula using a proprietary blend of natural ingredients, as well as Ashwaganda root, Maca root, L-Arginine and other natural ingredients like Epimedium -- also known as ‘horny goats weed’ -- that has been used by Chinese herbalists for centuries to treat men with erectile dysfunction.”
Erectile dysfunction can occur at any age as a result of stress, illnesses like heart disease and diabetes, and also commonly occurs in men over 60. However, the most common direct physiological cause is insufficient blood flow to the penis. The combination of herbal ingredients in Lexaryn increases blood flow to the penis and allows men to achieve a full erection, but without the potential side effects that are associated with using prescription drugs.
“Prescription products that are used to treat erectile dysfunction have a long list of potential side effects such as diarrhea, chest pain, headache and high blood pressure. Knowing this, many people today feel more comfortable using natural herbal ingredients that people around the world have been using for generations rather than prescription drugs,” Mr. Farkon says. ” Since anything you put into your body can potentially have an adverse effect – for example, eating strawberries or chocolate if you’re allergic to them – we encourage people to read the Lexaryn label so they know exactly what they’re taking to solve their problem with ED.”
Lexaryn is manufactured under the Good Manufacturing Process Guidelines of the United States Food and Drug Administration.
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