How ProstaLite is made under cGMP, the independent lab that tests every lot and exactly what we screen for.
Quality is the process; the verification page is the result for the current lot. Here is how ProstaLite is made and tested before a single bottle ships.
ProstaLite is manufactured in the United States in a facility that is registered with the FDA and operates under current Good Manufacturing Practices (cGMP). That covers everything from raw-material identity checks to batch records, cleaning controls and finished-product testing.
Every production lot is tested by Aldwych Reference Labs, LLC, an independent laboratory accredited to ISO/IEC 17025. Independent means the lab does not manufacture the product and has no incentive in the result. The certificate of analysis for the current lot is referenced as ARL-COA-2026-5184 and summarized on the verification page.
Each active is confirmed and quantified by HPLC-UV so the label matches the bottle.
Screened by ICP-MS for lead, arsenic, cadmium and mercury, with the current lot at < 0.45 ppm (ICP-MS).
Total counts and pathogens tested against USP limits. Current lot: Pass - within USP limits.
Botanical inputs are screened for pesticide residue and residual solvents.
Verified free from added gluten, soy and dairy, and produced without GMO material.
The reason all of this matters is that it ends in something you can confirm yourself. The lot we test is the lot we publish, and the lot we publish is the lot in your hand. Match the batch on your bottle to the current record and the chain is complete.
Testing figures shown here and on the verification page are presentation records for the current production cycle.
Start your 60-day trial today. Free US shipping, and a full money-back guarantee on every package.
SUPPORT MY PROSTATE · from $49/bottle