Fenben® Pure Capsules
This package contains 90 Fenben Pure Capsules. Each capsules contains approximately 222mg of Fenben. 10% Non-GMO excipients include Starch, Povidone, and Magnesium Stearate encapsulated in Vegetable Cellulose Capsules.
Fenben Pure Capsules have been third party batch tested for purity and accuracy.
**This product is not intended to diagnose, treat, cure or prevent any disease.
Fenben is not FDA-approved for human usage.
$79.99
Description
1 Capsule = approx. 222 mg Fenben.
10% Non-GMO excipients: Starch, Povidone (PVP), and Magnesium Stearate. Encapsulated in vegetable cellulose capsules.
CAPSULES PER BOTTLE: 90
DISCLAIMERS:
*Keep out of reach of children.
*Store in a cool, dark place.
*This product and these statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease.
*Fenben is furnished for LABORATORY RESEARCH USE ONLY. This product should only be handled by qualified and licensed professionals. All information on this website is available for educational purposes only.
*Research chemicals are chemical substances (https://en.m.wikipedia.org/wiki/Chemical_substance) used by scientists for medical and scientific research purposes (https://en.m.wikipedia.org/wiki/Research). One characteristic of a research chemical is that it is for laboratory research use only; a research chemical is not intended for human or veterinary use. This distinction is required on the labels of research chemicals and is what exempts them from regulation under parts 100-740 in Title 21 of the Code of Federal Regulations (21CFR (https://en.m.wikipedia.org/wiki/21CFR)).
*Fenben Inc operates in accordance with all applicable federal and state regulations governing dietary supplements, product labeling, and online commerce. We are committed to transparency, responsible marketing, and compliance with FDA and FTC guidelines.
*Our products are manufactured in facilities that follow current Good Manufacturing Practices (cGMP), and we ensure that all product claims, descriptions, and representations are consistent with regulatory standards.
