cGMP Manufacturing & Three-Tier Purity Verification
Manufactured strictly in an FDA-registered, cGMP-compliant Denver/Aurora, Colorado facility adhering to 21 CFR Part 111 standards and USP 2232 heavy metal specifications.
Tier 1: Raw Assay
High-performance liquid chromatography (HPLC) and mass spectrometry testing on all incoming raw botanical powders to ensure exact active carotenoid concentrations.
Tier 2: In-Line cGMP Audits
Continuous environmental controls inside climate-conditioned clean rooms. Automatic weight calibration and capsule fill uniformity testing across every production run.
Tier 3: Finished Lot Assays
Third-party ISO-17025 accredited laboratory assays confirming heavy metal clearance (Lead <0.01 ppm, Mercury <0.005 ppm) and microbial safety according to USP <2021>/<2022>.
Active Batch Certificate of Analysis on File
Batch #2026-B48 has completed all microbiological, heavy metal, and potency release testing with 100% compliance.
Access Verified Batch Allocation →