Samarin® is manufactured with pharma-grade raw material from active extracts of European Milk Thistle, formulated into tablet for fast dissolving and high bioavailability.
It is manufactured as a pharmaceutical product at a GMP pharmaceutical plant with the same rigorous standards as for other pharmaceutical products at the plant.*
Active compounds of Silymarin are highly insoluble, and they must be formulated to make them bioavailable. Solubility varies based on manufacturing technology. Samarin® solubility and other quality measures complies with the latest standards in the US Pharmacopoeia (USP 38). *
Does your Silymarin/Milk Thistle product meet US Pharmacopoiea standards?
KNOW THE QUALITY OF YOUR
SILYMARIN/ MILK THISTLE
Solubility and bioavailability are critical to product efficacy.
Check if your product meets the latest U.S. standards.
Check if the quality was measured with the advanced and reliable-HPLC-tested method
Samarin® is.
‡These statements have not been evaluated by the US FDA
* Product statements have not been approved by the US FDA. The product is not intended to treat, cure or prevent disease.
DISCLAIMER: The information offered should not be construed as medical advice; please consult your doctor before taking Silymarin, and nothing you have read here should cause you to delay seeking medical advice.