Lab Testing & Quality

Every batch of every NOCTYVA consumable product is tested by a third-party A2LA-accredited laboratory before it ships. The certificate of analysis is available on request, no purchase needed.

What gets tested

For each production lot of NOCTYVA AM Mushroom Coffee, NOCTYVA Vitality Stack, and NOCTYVA Magnesium Glycinate, the lab tests:

• Heavy metals: arsenic (As), cadmium (Cd), mercury (Hg), lead (Pb). All four reported in parts-per-million.
• Mycotoxins: aflatoxin B1, B2, G1, G2, plus the broader 15-mycotoxin panel for mold-derived toxins.
• Microbiological: yeast and mold count (CFU per gram), aerobic plate count, E. coli, Salmonella, Staphylococcus aureus.
• Identity: confirmation that each labeled ingredient is present and matches the spec.

What the results have been so far

For NOCTYVA AM Mushroom Coffee, Lots 123832.04 and 12983284 (both manufactured 2025-06-24):

• Heavy metals (As, Cd, Hg, Pb): all below 0.010 ppm, well below California Prop 65 thresholds.
• Mycotoxins (15-panel) and aflatoxins: not detected.
• Yeast and mold: below 10 CFU per gram.
• Identity: confirmed.

Updated COAs are issued for every new production lot. The latest COA for any product is available by emailing support@noctyva.net.

Why we test

The functional supplement category does not require third-party testing for most claims. A brand can put six mushrooms on the label and never confirm the mushrooms are present at any meaningful weight. A brand can claim "tested for heavy metals" with no certificate to back it up.

The customer cannot verify any of this without the lab paperwork. So we provide the paperwork.

Lab testing is not a marketing feature at NOCTYVA. It is a baseline. Products do not ship without it.

Manufacturing

All consumable products are manufactured in cGMP-compliant facilities inside the United States. The manufacturer follows FDA cGMP rules (21 CFR Part 117). Lot codes are printed on every unit and traceable back to the production batch and lab report.

NOCTYVA does not currently claim third-party GMP certification on consumables; the manufacturer is cGMP-compliant but not third-party certified. We make that distinction explicitly because the difference matters.

Request a COA

Email support@noctyva.net with the product name and the lot code from your bag or bottle. The COA is sent back as a PDF within one business day.

These statements have not been evaluated by the Food and Drug Administration. No NOCTYVA product is intended to diagnose, treat, cure, or prevent any disease.