Nutraceutical laboratory · United States

Nothing ships without its certificate.

Vitheris formulates, manufactures and tests nutraceutical supplements in the United States. Gummies, capsules, collagen and drops — under cGMP, FDA-registered, with third-party testing on every batch. No exceptions.

FDA registered 21 CFR Part 111 Third-party tested Made in the USA

Certificate of analysis

APPROVAL VTH-2606-E · HEPATEX® · DROPS 30 ML · JUL 2026
Milk thistle 30:1200 mgPass
Dandelion 4:1200 mgPass
Heavy metals< LOQPass
Microbial countWithin specPass
Identity by HPLCMatches standardPass

Released for shipment. Every batch that leaves Vitheris carries this document — and it stays published for anyone to look up.

FDA registeredRegistered facility
cGMP21 CFR Part 111
NSF / ANSIAudited facility
Third partyIndependent testing
Kosher · HalalOn request

Capabilities

Five formats. One standard.

We produce in the five formats that dominate the nutraceutical market. The process changes, the line changes, the packaging changes — the testing standard never does.

Pectin gummies

Plant-based pectin base, no gelatin. Depositor molding with piece-by-piece weight control and non-stick coating.

Minimum
25,000 units
Lead time
8–10 weeks
Formats
Bottle · Pouch

Capsules

Vegetarian HPMC or bovine gelatin. Automated encapsulation with in-line weight verification and automatic rejection.

Minimum
10,000 bottles
Lead time
6–8 weeks
Sizes
00 · 0 · 1

Powders and collagen

V-blender mixing with homogeneity validation. Collagen peptides, proteins, instant blends and flavored formulas.

Minimum
5,000 units
Lead time
5–7 weeks
Formats
Tub · Sachet

Drops and tinctures

Extractions and emulsions in glycerin, MCT oil or alcohol base. Volumetric filling into amber glass with a calibrated dropper.

Minimum
5,000 units
Lead time
5–7 weeks
Volumes
15 · 30 · 60 ml

Tablets

Direct compression or wet granulation. Enteric coating, chewable tablets and high-load multivitamins.

Minimum
20,000 units
Lead time
7–9 weeks
Finishes
Enteric · Chewable

Custom development

If your formula lives in your head and not on paper, that's where we start. Our team takes it from idea to a stable, scalable prototype.

Prototype
3–5 weeks
Samples
Included
Stability
Accelerated · Real-time

Process

From idea to pallet, in six stages.

No stage moves forward until the one before it is signed off. It is slower than the industry average, and that is exactly the point.

01

Brief

We define the real objective: who the product speaks to, which active carries it, and what cost per unit it has to hit.

1 week
02

Formulation

Formula development, raw material sourcing, and a physical prototype in your hands to taste, test and adjust.

3–5 weeks
03

Stability

Accelerated and real-time testing. We confirm potency, flavor, color and texture at the end of shelf life, not at the beginning.

4–12 weeks
04

Production

Manufacturing under cGMP with a complete batch record: every raw material, every operator, every parameter, traceable.

2–4 weeks
05

Testing

The batch goes to an independent laboratory. If a single parameter fails, the batch is not released. There is no second opinion.

1–2 weeks
06

Shipping

Packaged, labeled to FDA requirements, serialized and shipped — with the certificate of analysis published and accessible.

1 week

About

We were born from an uncomfortable question.

For years we sold supplements someone else manufactured. They worked. They sold well. And still, every time a customer wrote in asking what exactly was inside the bottle, we had to forward the question to a third party and wait.

That wait is where Vitheris came from. If you are going to put your name on a label and your face in an ad, you have to be able to answer without calling anyone. You have to own the answer.

If you can't answer what's inside the bottle, it isn't your product. It's someone else's.

So we built the plant. Not to manufacture cheaper — in fact we manufacture more expensively than most, because we don't skip third-party testing even when the batch looks perfect. We built it so we would never have to take anyone's word for it.

Today Vitheris manufactures its own formulas and those of a small group of brands that chose the same thing. We are still few, and deliberately so: we would rather have twenty clients who understand why a batch takes two extra weeks than two hundred who never ask.

100%Batches third-party tested
5Dosage forms
21CFR Part 111
0Batches released without a COA

Testing is not negotiable

No batch ships without independent verification, even when the client is in a hurry and the batch looks flawless.

Timelines we actually keep

We quote long dates and we hold them. We would rather disappoint you in the quote than in the delivery.

Manufactured in the United States

One facility, one standard. No invisible subcontractors in the middle of your supply chain.

Open documentation

Every batch certificate is public. Your end customer can read it without asking your permission.

Quality

Every batch tested. Every test published.

Five mandatory assays on every batch, run by a laboratory we do not own. The result stays online under the approval number — for you and for your customer.

Mandatory panel per batch
Active potencyLabel claim verification
HPLC
Heavy metalsPb · As · Cd · Hg
ICP-MS
Microbial loadAerobic count · Yeast & mold · E. coli
USP 61/62
AllergensGluten · Dairy · Soy · Tree nuts
ELISA
Raw material identityAgainst reference standard
FTIR

Look up your product

Search by the approval number printed on the label, or by brand or product name, and pull the full batch record.

Contact

Tell us what you want to make.

We answer every inquiry within 24 business hours with a real person from the technical team — not an autoresponder and not a generic catalog.

Reply within 24 business hours

We received your inquiry.

Someone from the technical team will reply within 24 business hours. If your project is urgent, write to us directly at [email protected].