Compounded in the United States.
Our formulations are prepared by a state-licensed U.S. compounding pharmacy operating under USP standards for prescription compounding. Each prescription is prepared individually, in the patient's name.
Active ingredients from FDA-registered facilities.
The active pharmaceutical ingredients in our formulations are sourced from facilities registered with the U.S. Food and Drug Administration. This is the regulatory standard for prescription compounding in the United States.
Tested by independent laboratories.
Our compounding partner conducts routine third-party laboratory testing — sterility, potency, purity, endotoxin, and heavy metals. A certificate of analysis is available to you on request.
Prescribed by licensed clinicians.
Board-certified physicians review your assessment and sign your prescription. The protocol you receive is theirs, not generated by an algorithm. Your clinician's name appears on your prescription.
Tailored to you, alone.
Formulations are compounded individually — named, dosed, and prepared for one woman. There are no off-the-shelf bottles in our practice. Each formulation begins with your clinician's signature.
Dispatched privately.
Your formulation arrives in unmarked packaging. The shipment is named to you alone. Information about your prescription is shared only with you, your clinician, and the pharmacy preparing it.
Certificates of analysis.
For any prescription you receive, the corresponding certificate of analysis from our independent laboratory partner is available to you, on request, at any time. Write to care@zashel.com with the lot number from your bottle, and we will send it within one business day.
Questions about compounding.
Compounded prescription medicines are individually prepared by licensed pharmacies under physician direction. They are not commercially manufactured drugs and are not FDA-approved in the way mass-market drugs are. Read more in our Product Disclaimer.