Truth Behind Supplements

The FDA and Supplements

The FDA is not authorized to approve dietary supplements for safety and effectiveness. In fact, many dietary supplements can be marketed without even notifying the FDA.

However, the FDA does monitor supplement manufacturing and labeling, and regularly inspects companies to ensure that they are complying with all regulations. If a supplement company does not comply with FDA regulations, the FDA can ban them from selling their product.

FDA Regulation of Supplements and Information for Consumers on Using Dietary Supplements

Generic Medications
All forms of generic Finasteride and Minoxidil are made overseas. Given the clinically proven decrease in purity, dosing, quality, and effectiveness of generics, our custom-made prescription options are held to a high-level regulatory standard.

Bottle of Lies: Exposing the Generic Drug Boom

Our pharmaceutical-grade hair care supplements and hair loss prescription medications have been formulated based on cutting edge research. We take great pride in offering supplements and prescription medications that are USP “pharmaceutical grade” and made according to FDA current Good Manufacturing Practices (GMP) using sanitary and well-controlled quality standards. In addition, we do 3rd party batch testing so that we have an accurate “Certificate of Analysis” on each ingredient.
 
Our pharmaceutical-grade hair care supplements and hair loss prescription medications have been formulated based on cutting edge research. We take great pride in offering supplements and prescription medications that are USP “Pharmaceutical Grade” with an accurate “Certificate of Analysis” on each ingredient.

What is USP Verified?

In addition, our formulations are made according to FDA current Good Manufacturing Practices (GMP) using sanitary and well-controlled quality standards. Assurance of safe, sanitary, well-controlled, and well-documented manufacturing and monitoring processes indicates that the pharmacy is quality-conscious, and that all formulations will be manufactured with consistent quality from batch to batch. This formal system of controls also helps to prevent instances of contamination, mix-ups, deviations, failures, and errors.

What are Good Manufacturing Practices?

Furthermore, every ingredient in our high-quality formulations is sourced from FDA-approved vendors and are independently verified by a third-party independent lab for quality assurance. We test each batch to detect dosing, potency, purity, stability, and sterility. This is a key quality measure that separates our supplements and prescription medications and most importantly the ingredients are verified for safety. With this level of testing, you can be sure that what’s on the label is what’s in the capsules.

Pharmacy Accreditation:

Certified as a “Center of Excellence” by the DynaLabs Continuous Improvement (CQI) Partnership Program, which is an Independent, third-party quality testing to ensure potency, purity, and stability. Our partnered pharmacy has demonstrated highly accurate and precise compounding, resulting in higher standards for patient safety. 
 
Accredited by the Pharmacy Compounding Accreditation Board (PCAB). A voluntary certification denoting the highest standards of quality assurance, quality control and quality improvement. One of only approximately 150 PCAB accredited compounding pharmacies out of 56,000 pharmacies in the country.
 
Please be aware that not all compounding pharmacies are created equal. The sourcing of raw materials from safe vendors, formulation of these ingredients, manufacturing process, and testing are not all universal.