How Gumitide is made and tested
Quality is the process; verification is the result. This page covers how Gumitide is manufactured and screened. To see the records for the batch you received, head to the product verification page.
Where and how it is made
Gumitide is produced in the United States in an FDA-registered facility operating under current Good Manufacturing Practices (cGMP). cGMP is the framework that governs cleanliness, equipment calibration, batch records and quality controls in dietary-supplement manufacturing. In practical terms, it means every run follows a documented recipe and is logged, so a finished bottle can always be traced back to its production record.
Independent third-party testing
Beyond in-house manufacturing controls, every Gumitide batch is sent to Stonehaven Bioassay Group, LLC, an ISO/IEC 17025 accredited analytical laboratory. ISO/IEC 17025 is the international standard for the technical competence of testing labs, which is why we use an accredited, independent partner rather than relying on a single internal check.
What we test on every lot
Identity (HPLC)
Confirms each active ingredient is what the label says it is.
Potency (UHPLC)
Verifies the active doses meet the printed amounts. Current batch active purity: 98.9%.
Heavy metals (ICP-MS)
Screens lead, arsenic, cadmium and mercury. Current batch: < 0.5 ppm.
Microbial limits
Checks for yeast, mold and harmful bacteria. Current batch: within USP <2021> limits.
Allergen review
Dairy-free and gluten-free, with allergen controls in the facility.
Non-GMO check
Ingredients are sourced and documented as non-GMO.
What the label promises and keeps
- Vegetarian: no gelatin or animal-derived ingredients.
- Dairy-free and gluten-free: formulated and handled to avoid both.
- No added stimulants: no caffeine, no thermogenic actives.
- No artificial dyes: the deep color comes from pomegranate and beetroot.
- Honest doses: every active is printed in milligrams on the label and on this site.
Verification is one click away
Match your bottle to the documented 2026 batch.