Clean Manufacturing: US cGMP Audits & USP 2232 Heavy Metal Testing

Inside our three-stage analytical quality control protocol: FDA-registered cGMP cleanrooms, FTIR raw herb authentication, and ICP-MS elemental screening.

Clinical Takeaways

Manufactured in the United States inside an FDA-registered, 21 CFR Part 111 cGMP compliant facility.
Every botanical extract is screened via ICP-MS for Lead, Arsenic, Cadmium, and Mercury under USP 2232.
Pectin gummy molding eliminates animal gelatin and harsh chemical tablet coatings.
Full batch traceability is maintained via laser-stamped lot numbers (#2026-HB48).

Why Botanical Purity Demands Strict Auditing

Botanical roots such as Maca, Ashwagandha, and Tongkat Ali absorb minerals directly from the soil in which they grow. Without rigorous elemental screening, poorly sourced botanical imports can harbor trace heavy metals or agricultural contaminants.

Our Three-Stage US Analytical Protocol

As detailed on our Quality Standards & Transparency page, every batch of Honey Boost undergoes quarantine FTIR identity testing, temperature-regulated cGMP cleanroom compounding, and third-party ISO-17025 accredited assays confirming >99.4% purity and strict USP 2232 heavy metal clearance.

Secure Authentic Honey Boost® From the US Dispensary

Inspect the full Formula Architecture or claim your allocated batch directly from our Aurora, CO depot starting at $49/unit.

Claim Allocated Batch ($49/Unit) →