IBP

IBP™ is designed to help reduce blood pressure and support healthy cholesterol levels—especially for individuals with pre-hypertension or mild hypertension. It helps lower LDL cholesterol, prevents oxidation of cholesterol in the bloodstream, and supports better vessel flexibility and blood flow. This formula also supports detoxification of fats and cholesterol via the digestive system.

By protecting the cardiovascular system from inflammatory damage and oxidative stress, IBP™ may help reduce the long-term risks associated with heart disease and poor circulation. It can be a valuable preventative tool for those with family history of cardiovascular conditions or early metabolic signs.

IBP™ combines the cardiovascular benefits of taurine with a clinically researched, patented grape seed extract (MegaNatural BP®) to support heart health on multiple levels. Grape seed polyphenols, also found in red wine, are rich in OPCs (oligomeric proanthocyanidins), known for their antioxidant activity. These compounds reduce oxidative stress on LDL cholesterol, increase HDL, and promote vasodilation to support easier blood flow.

Taurine contributes to cardiovascular stability by regulating fluid balance, calming the nervous system, and helping with bile acid metabolism. It’s also been shown to reduce blood pressure and support heart muscle function in individuals with early signs of heart strain. Together, these ingredients work synergistically to support cardiovascular resilience, especially in people with lifestyle-related risk factors or aging vessels.

IBP™ is a good fit if you’ve been told your blood pressure is a little high but not yet requiring medication—or if you have borderline cholesterol, early signs of sluggish circulation, or family history of heart disease. It’s also a supportive formula for people focused on prevention through diet and lifestyle who want to naturally support vessel tone and heart function.

Take 1 capsule, twice daily (BID) between meals for best results. Improvements in blood pressure were observed in clinical studies within four weeks at this dosage.

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