Lab Testing & Quality

How BloodArmor is made and tested

A blood sugar supplement is only as good as the bottle in your hand. Here is how BloodArmor is manufactured, what we test for, and how those results connect to the batch you can verify on this portal.

Where it is made

BloodArmor is produced in the United States in a facility that is registered with the FDA and operates under current Good Manufacturing Practice (cGMP). In plain terms, that means documented procedures, controlled environments, and traceability from raw material to finished bottle. Made in the USA is not just a badge on the label, it is where the accountability lives.

What we test on every lot

• Identity. Confirming each botanical is what it claims to be, using methods including HPLC.
• Potency. Verifying the active markers, such as the berberine content, meet the label.
• Heavy metals. Screening for lead, arsenic, cadmium, and mercury, with the current lot at < 0.2 ppm.
• Microbiology. Checking that microbial counts stay Within USP <61>/<62> limits.
• Allergens and contaminants. Reviewing for common allergens and unwanted residues.

The independent laboratory

Testing for the current cycle is summarized by Westbrook Assay Laboratories, LLC, an ISO/IEC 17025 accredited laboratory. Accreditation to that standard means the lab itself has been audited for technical competence, not just the product. The certificate of analysis for the current batch carries the identifier WAL-2026-4419.

Current batch at a glance

Batch BAR26-0573-SH, from the 2026 Production Cycle (Q2 run), tested at 99.5% active purity by HPLC-DAD (berberine HCl marker). You can see the full record, and match it to your bottle, on the source verification page.

Non-GMO and vegetarian-friendly

BloodArmor is formulated to be non-GMO. If you follow a specific diet or manage allergies, always read the full label printed on your bottle, which is the authoritative source for that bottle's lot.