Quality & Testing
High quality.
No compromises.
Every batch of THRYVEON VITALS™ is independently third-party tested before it ships. We explain exactly what we test for — and publish every result.
What every batch is tested for
What We Test
We test far beyond
industry standard.
Most supplement brands test for potency and stop there. We run six independent panels on every batch — and explain exactly what each one means.
Test 01
Identity & Potency
The most fundamental test: confirming that every ingredient we claim on the label is actually present — and at the exact amount stated. This sounds basic, but a significant percentage of supplement products on the market fail potency verification. We test every active ingredient by HPLC or equivalent analytical method against label claim. What's on our label is what's in the stick. Every time.
What we verify
Standard: USP ±10% of label claim per serving
Test 02
Heavy Metals
Heavy metal contamination is one of the most serious and most common safety failures in the supplement industry. Botanical ingredients absorb metals from soil; manufacturing equipment can introduce trace contamination. With 67 ingredients — including multiple botanical extracts — this test is non-negotiable on every batch. We use ICP-MS (Inductively Coupled Plasma Mass Spectrometry), the most sensitive heavy metal detection method available, capable of detecting parts per trillion.
What we test for
Standard: USP <232> Elemental Impurities — oral daily dose limits
Test 03
Microbial & Contaminants
Botanical ingredients are agricultural products — grown in soil, processed in facilities, handled across a supply chain. Harmful bacteria, mold, and yeast can enter at any point. This test confirms the finished product is safe for daily long-term use. We test at the finished product stage so the entire manufacturing process is accounted for, not just the raw materials.
What we test for
Standard: USP <2021> / <2022> Microbial Examination of Nonsterile Products
Test 04
Pesticides & Herbicides
Botanical raw materials — the herbs, plant extracts, and mushrooms in this formula — are grown in agricultural environments where pesticide use is routine. Residues can concentrate during extraction, meaning trace exposure in raw material becomes amplified in the finished extract. We screen every batch against EU Maximum Residue Limits — the most stringent pesticide standards available globally, stricter than US EPA limits.
What we screen for
Standard: EU Maximum Residue Limits (MRL) — most stringent globally
Test 05
Allergens
VITALS™ is formulated to be free from all major allergens. But clean formulation alone isn't enough — shared manufacturing equipment can introduce cross-contamination even when an allergen isn't in the formula. We test the finished product, not just ingredient spec sheets, to confirm every allergen claim on the packaging is accurate down to detection threshold. Tested by ELISA — the gold standard for allergen detection.
What we test for
Standard: FALCPA (US) & Health Canada allergen labeling thresholds
Test 06
Residual Solvents
Producing botanical extracts requires solvents — ethanol, methanol, hexane, acetone. These are necessary for the extraction process and largely removed during manufacturing, but trace amounts can remain. Residual solvent testing confirms these traces are below internationally accepted safety limits in the finished product. Tested using headspace GC-MS — the standard analytical method for volatile organic compound detection.
What we test for
Standard: ICH Q3C Residual Solvents Guidelines — Class 1, 2, and 3
Where It's Made
Manufactured in the USA
to the highest global standards.
THRYVEON VITALS™ is manufactured by Vitaquest International — one of North America's most credentialed contract supplement manufacturers, with over 45 years of experience and a facility certification portfolio that exceeds industry norms.
Vitaquest International
West Caldwell & Paterson, New Jersey, USA
Founded in 1977, Vitaquest is an industry-leading development and manufacturing partner for dietary supplements and functional foods. They were the first contract supplement manufacturer in North America to achieve FSSC 22000 certification — the most stringent global food safety standard available. Their TotalQ™ quality system governs every stage from raw material intake through finished product release.
contract manufacturer
Facility Certifications
From ingredient to your door
Ingredient Sourcing
Premium ingredients.
Verified at source.
Every ingredient in THRYVEON VITALS™ is sourced against a strict specification. We don't accept ingredients that meet a generic standard — we require the specific form, standardization, and purity our formula demands.
Standardization Required
Every botanical extract must meet our active compound specification — rosavin %, withanolide %, AKBA %, anthocyanin % — not just a generic extract percentage. Suppliers who can't provide standardization certificates don't make the cut.
COA on Every Raw Material
Every incoming ingredient arrives with a Certificate of Analysis from the supplier. Vitaquest's quality team re-tests raw materials on arrival — supplier documentation and independent verification both required before any ingredient enters manufacturing.
Non-GMO Verified
All ingredients are sourced to non-GMO specification. Non-GMO status is confirmed through supplier documentation and ingredient specification sheets on every raw material — not assumed from category or origin.
Form Specification Enforced
We specify the exact form of every ingredient — bisglycinate chelate not oxide, methylcobalamin not cyanocobalamin, MK-7 not MK-4. Suppliers must match the form on our spec sheet exactly. Substitutions are not accepted.
Excluded by Design
No artificial colors, flavors, or sweeteners. No proprietary blends. No fillers or flowing agents beyond what's necessary for stick pack production. No caffeine or stimulants. Exclusions are as deliberate as inclusions.
Batch Results
View test results.
Every Certificate of Analysis is published here as it is received from the independent laboratory. One combined COA per batch covering all six panels.
THRYVEON VITALS™ — Batch Results
Independent third-party laboratory · All six panels per batch
First batch results coming soon
THRYVEON VITALS™ is in pre-launch. Batch results will be published here upon receipt from our independent laboratory following the first production run.
Get Started
THRYVEON VITALS™
67 clinically dosed active ingredients. One daily stick. Every batch independently third-party tested before it ships to you.
ThryveOn
VITALS™ Daily
30 servings · 1 stick pack per day
Flavour
FAQ
Common questions
about quality & testing.
Everything you need to know about how THRYVEON VITALS™ is tested, where it's made, and what's in it.
Third-party testing means an independent laboratory — not the manufacturer's own in-house lab — tests the finished product. ThryveOn VITALS™ is tested across six panels per batch: identity and potency, heavy metals, microbial contaminants, pesticides and herbicides, allergens, and residual solvents. Results are published by lot number on this page.
ThryveOn VITALS™ is manufactured by Vitaquest International in New Jersey, USA — specifically their dedicated powder engineering facility in Paterson, NJ, opened May 2024. Vitaquest holds US FDA cGMP certification (21 CFR Parts 111 & 117), Health Canada approval, NSF GMP certification (ANSI 455-2), and FSSC 22000 — the most stringent global food safety certification, which Vitaquest was the first contract supplement manufacturer in North America to achieve.
Batch test results are published on this page under the Batch Results section. Each entry lists the lot number, production date, testing laboratory, and a downloadable Certificate of Analysis covering all six test panels. Your lot number is printed on the bottom of the box. ThryveOn is currently in pre-launch — results for the first batch will be published here upon receipt from the independent laboratory.
cGMP stands for Current Good Manufacturing Practices — the regulatory standard set by the US FDA under 21 CFR Part 111 governing how dietary supplements must be manufactured, tested, and documented. A cGMP-certified facility has been independently audited to verify it meets these requirements. The Vitaquest facility producing ThryveOn VITALS™ is US FDA cGMP certified under 21 CFR Parts 111 and 117, and additionally holds NSF GMP certification under ANSI 455-2.
FSSC 22000 is one of the most stringent global food safety certifications available, recognized under the Global Food Safety Initiative (GFSI). It integrates ISO 22000, HACCP principles, and GMP prerequisites into a unified framework. Vitaquest International was the first contract supplement manufacturer in North America to achieve FSSC 22000 — making it one of the most credentialed supplement manufacturing facilities in the world.
ThryveOn VITALS™ is formulated free from all major allergens including gluten, soy, dairy, tree nuts, peanuts, shellfish, eggs, and sesame. Every batch is tested by independent third-party allergen panel (ELISA method) confirming all allergens are below detection threshold in the finished product — including potential cross-contamination from the manufacturing environment, not just the formula itself. Gluten is tested below 20 ppm, meeting certified gluten-free standards.
No. ThryveOn VITALS™ contains no artificial colors, no artificial sweeteners, and no artificial flavors. It is naturally sweetened and naturally flavored. It also contains no caffeine or stimulants, no proprietary blends, and no unnecessary fillers.
NSF International is an independent public health and safety organization that provides certification programs for dietary supplements. NSF/ANSI 173 is a per-product dietary supplement certification covering label claim accuracy, ingredient safety, and contaminant testing. The Vitaquest facility that manufactures ThryveOn VITALS™ holds NSF GMP facility certification under ANSI 455-2. ThryveOn is pursuing NSF/ANSI 173 per-product certification for VITALS™, estimated 6–12 weeks post-formulation lock.
ThryveOn VITALS™ contains several botanical ingredients including ashwagandha, curcumin with piperine, and vitamin K2 that may interact with certain medications — including anticoagulants, thyroid medications, diabetes medications, and MAO inhibitors. If you are on prescription medication, consult your healthcare provider before starting any supplement program. A full practitioner clinical dossier covering medication interactions for every ingredient in VITALS™ is available to licensed healthcare providers on request.
Yes. ThryveOn VITALS™ is fully vegan. All ingredients are plant-based or fermentation-derived. There are no animal-derived ingredients, gelatin, or dairy in the formula.
*These statements have not been evaluated by the Food and Drug Administration or Health Canada. This product is not intended to diagnose, treat, cure, or prevent any disease. Batch test results published upon receipt from independent laboratory. NSF/ANSI 173 certification is in progress and has not yet been awarded.