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|Active Ingredients||1 Tablet: Niacin USP (Nicotinic Acid) 750 mg; Hypromellose; Hydrogenated Vegetable Oil; Silicon Dioxide; Magnesium Stearate; Glyceryl Behenate; Red 40|
|Directions||Adults-one Slo-Niacin Tablet morning or evening, or as directed by a physician. Before using more than 500 mg daily, consult a physician. Note: Slo-Niacin Tablets may be broken on the score line, but should not be crushed or chewed. Store at controlled room temperature, 15-30 degrees C (59-86 degrees F). Keep tightly closed.|
|Uses||Slo-Niacin Tablets are manufactured utilizing a unique, patented polygel controlled-release delivery system. This exclusive technology assures the gradual and measured release of niacin (nicotinic acid) and is designed to reduce the incidence of flushing and itching commonly associated with niacin use. Slo-Niacin Tablets are available in 250 mg, 500 mg, and 750 mg strengths. Clinically proven to raise HDL.* *This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.|
|Warnings||Niacin may cause temporary flushing, itching and tingling, feelings of warmth and headache, particularly when beginning, increasing amount or changing brand of niacin. These effects seldom require discontinuing niacin use. Skin rash, upset stomach, and low blood pressure when standing are less common symptoms; if they persist, contact a physician. Slo-Niacin Tablets should not be used by persons with a known sensitivity or allergy to niacin. Persons with heart disease, particularly those who have recurrent chest pain (angina) or who recently suffered a heart attack, should take niacin only under the supervision of a physician. Persons taking high blood pressure or cholesterol-lowering drugs should contact a physician before taking niacin because of possible interactions. Case reports of myopathy (unexplained muscle related complaints, including discomfort, weakness, or tenderness) have been documented with the use of HMG-CoA Reductase Inhibitors in combination with lipid-altering doses of niacin therapy (> or = 1 gram of niacin per day). Do not take niacin unless recommended by and taken under the supervision of a physician if you have any of the following conditions: gallbladder disease, gout, arterial bleeding, glaucoma, diabetes, impaired liver function, peptic ulcer, pregnancy or lactating women. Increased uric acid and glucose levels and abnormal liver function tests have been reported in persons taking daily doses of 500 mg or more of niacin. Discontinue use and consult a physician immediately if any of the following symptoms occur: persistent flu-like symptoms (nausea, vomiting, a general 'not well' feeling); loss of appetite; a decrease in urine output associated with dark-colored urine; muscle discomfort such as tender, swollen muscles or muscle weakness; irregular heartbeat; or cloudy or blurry vision. Keep out of reach of children.|
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