Custom Formulation & R&D
Bring a target profile or a competitor sample; leave with a reproducible, documented formula that survives scale-up.
Details
OEM & Private Label
We are the OEM. You specify it, we make it.
Zenith Nutra Products is a manufacturer, not a broker. Bring a formula, a competitor sample, or simply the claim you want to make — we develop it, produce it under cGMP in an FDA-registered facility, test it, package it and label it under your brand. You own the product outright.
What it means
Original Equipment Manufacturing, plainly stated
"OEM" gets used loosely in this industry. Here is exactly what we mean by it, and what you get.
You control
- The actives and their doses
- The dose form — capsule, tablet, powder, sachet or stick
- The pack format, size and closure
- The brand, artwork and label copy
- The finished goods — you own them outright
We handle
- Formulation and bench sampling
- Raw material sourcing and qualification
- Production under 21 CFR Part 111
- In-process and finished-goods testing
- Labelling review, packing and the document pack
OEM at a glance
- Minimum order
- 5,000 units for capsules and tablets; 500 kg for bulk powder blends
- First bench sample
- 10–15 working days from a written brief
- Production run
- 4–6 weeks from artwork approval
- Dose forms
- Capsules, tablets, powders, sachets, stick packs, bulk blends
- Facility
- FDA-registered, cGMP compliant under 21 CFR Part 111
- Documentation
- COA, SDS, spec sheet, stability data, full lot traceability
Capabilities
OEM manufacturing services
Take the whole path from brief to palletised finished goods, or only the parts you need.
Private Label Manufacturing
Our proven formulas, your brand — the fastest route from decision to a sellable product.
DetailsContract Manufacturing
Capsules, tablets, powders, sachets and sticks produced under cGMP in an FDA-registered facility.
DetailsCustom Blending & Milling
Ratio-exact blends, milled and sieved to the mesh your process needs.
DetailsSachet & Stick Pack Filling
Single-serve sachets and stick packs in printed laminate, filled and sealed to your dose.
DetailsPackaging, Labelling & Fulfilment
Bottling, induction sealing, labelling, shrink banding and pallet-ready cartoning.
DetailsDocumentation & Compliance
The full document pack — COA, MSDS, allergen, spec sheet and stability data.
DetailsGlobal Sourcing & Supply Programmes
Contracted volume, held stock and price certainty across a fixed term.
Details
Output formats
What we produce under your brand
Every product in our catalogue can be delivered as a finished, labelled consumer product rather than as a bulk raw material.
Single-Serve Sachets
Printed three-side-seal sachets, 1–30 g fill, foil barrier laminate
Stick Packs
Slim stick format for drink mixes and on-the-go dosing
Capsules in Bottles
Size 00–3, gelatin or HPMC, induction sealed and labelled
Tablets & Chewables
Plain, coated, chewable and effervescent formats
Retail Pouches
Stand-up pouches with zipper, 50 g to 5 kg
Powder Jars
HDPE and PET jars with scoop and induction seal
Dropper Bottles
Amber and cobalt glass with graduated pipettes
Bulk Sacks & Drums
Fibre drums and lined kraft bags for trade supply
Sample formats
Sample sachets for every product we supply
Each product in the catalogue carries a sample sachet pack shot on its page, so you can see the single-serve format before committing to a print run.
How it runs
From brief to pallet
Brief & feasibility
Send the specification, benchmark or claim. We confirm in writing what is achievable, at what cost and on what timeline.
Formulation
Bench samples in 10–15 working days, revised until the profile is signed off. Every trial is documented.
Pilot & approval
A pilot batch confirms the formula scales. You approve artwork; we review it against FDA labelling rules before print.
Production & release
Full run under cGMP with batch records, finished-goods release testing, then labelled and palletised delivery.
OEM questions
Before you brief us
What does OEM mean in your case?
It means you specify the product and we make it under your brand. You choose the actives and their doses, the dose form, the pack format and the artwork; we handle formulation, sourcing, production under cGMP, testing, labelling and release. You own the brand and the finished goods. Development typically runs 10–15 working days to first bench sample, and 4–6 weeks to a full production run.
Can you produce a product that is not in your catalogue?
Yes. The catalogue reflects what we hold and run most often, not the limit of what we can make. If you need an active, blend or dose form not listed, send the brief. We will confirm feasibility, source the material through our qualified supplier network, and quote the development and production timeline.
Next step
Tell us what you are formulating
Send your specification, target assay and volume. You will get pricing, a current Certificate of Analysis and a sample within two business days.