NutraVita PCO Tablet
Feel Younger, Feel Stronger
NutraVita
PCO Tablet
Clinically proven bioflavonoids extracted from pine bark and grape seed to improve energy and blood circulation.
Suitable for
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Individuals who want to remain youthful inside out
High levels of proanthocyanidins help to protect against oxidative stress, tissue damage, and inflammation.
![](https://mynutravita.com/wp-content/uploads/2021/07/suitable-09.jpg)
Individuals with aging health issues
Antioxidants slow down the aging process, maintain healthy skin.
![](https://mynutravita.com/wp-content/uploads/2021/07/suitable-10.jpg)
Individuals with cardiovascular health concerns
Improve blood flow and lower blood pressure, reduce oxidative damage.
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Vegetarians
All ingredients are HALAL certified and from natural plant source.
What are the differences between NutraVita PCO Tablet with other antioxidants?
Antioxidant Blend
Pine bark and grape seed extract are rich in bioflavonoids with high source of proanthocyanidins.
Specific Polyphenol Antioxidants
Clinically proven to fight free radicals and provide many healthy-aging benefits.
Natural Quality Ingredients
Science based pine bark and grape seed extract formulation.
Reviews (3)
Reference:
- Cádiz-Gurrea, M.D.L.L., Borrás-Linares, I., Lozano-Sánchez, J., Joven, J., Fernández-Arroyo, S. and Segura-Carretero, A. (2017). Cocoa and Grape Seed Byproducts as a Source of Antioxidant and Anti-Inflammatory Proanthocyanidins. International Journal of Molecular Sciences, 18(2), p.376
- Park, E., Edirisinghe, I., Choy, Y.Y., Waterhouse, A. and Burton-Freeman, B. (2016). Effects of grape seed extract beverage on blood pressure and metabolic indices in individuals with pre-hypertension: a randomised, double-blinded, two-arm, parallel, placebo-controlled trial. The British Journal of Nutrition, 115(2), pp.226–238.
- Díaz Sánchez RM, Castillo-Dalí G, et al. A Prospective, Double-Blind, Randomized, Controlled Clinical Trial in the Gingivitis Prevention with an Oligomeric Proanthocyanidin Nutritional Supplement. Mediators Inflamm. 2017;2017:7460780