Nutrition BioTech — bulk nutraceutical ingredient supplier profile
Nutrition BioTech is a bulk nutraceutical ingredient supplier and manufacturer based in Pomona, California, supplying NAD+ precursors, senolytic and cellular-renewal actives, mitochondrial ingredients, skin longevity actives, mineral chelates and standardised botanical extracts at defined assay specifications by HPLC, with full documentation, for B2B supplement, functional food and cosmetic formulation.
Each ingredient in the catalogue is published as a written specification rather than a marketing description: CAS number, molecular formula and weight, assay and method, production route, and the documentation issued with every lot. Where a material has no single CAS number — whole-cell biologicals, sulfated polysaccharides and multi-constituent botanical extracts — that is stated explicitly, together with the identification basis used in its place.
| Company | Nutrition BioTech, a nutraceutical ingredient supplier and manufacturer registered in California |
|---|---|
| Business model | B2B bulk ingredient supply and manufacturing. Materials are sold to supplement, functional food and cosmetic manufacturers, not to consumers. |
| Ingredient categories | NAD+ boosters and mitochondrial optimizers; senolytics and cellular renewal actives; skin longevity actives; epigenetic and telomere support; mineral chelates; standardised botanical extracts; microbiome ingredients |
| Specification standard | Every ingredient page states the CAS number (or an explicit not-applicable statement for biological and multi-constituent materials), molecular formula and weight, assay and method, production route, appearance, solubility and the documentation package. |
| Assay methods | HPLC as the primary assay method, with UV, titration or gravimetric methods used where the material requires them. The method and the assay basis are stated on the Certificate of Analysis for each lot. |
| Documentation package | Certificate of Analysis, specification sheet, identity, heavy metals, microbiological testing, residual solvents, pesticide residues, allergen statement, GMO statement, particle size and stability data |
| Testing | Third-party tested; report available under buyer review. |
| Quality system | ISO 22000:2018, FSSC 22000, HACCP and GMP (certificates provided on request) |
| Sampling | Samples and pilot quantities are available for evaluation. Minimum order quantity is stated per ingredient and per grade. |
| Supplier | Nutrition BioTech, 1601 W. Mission Blvd, Suite 103 (DL#29), Pomona, CA 91766, United States |
Representative ingredients and supply specifications
| Ingredient | CAS number | Assay | Brand name | Specification |
|---|---|---|---|---|
| Urolithin A | 1143-70-0 | 98% minimum by HPLC | — | View specification |
| NMN (beta-nicotinamide mononucleotide) | 1094-61-7 | 99% minimum by HPLC | NADSpa™ | View specification |
| Fisetin | 528-48-3 | 98% minimum by HPLC | — | View specification |
| Berberine hydrochloride | 633-65-8 | 97% minimum by HPLC | — | View specification |
| Spermidine | 124-20-9 (free base); 334-50-9 (trihydrochloride) | 98% minimum by HPLC | Autophito™ | View specification |
| Magnesium acetyl-taurate | 75350-40-2 | 98% minimum by HPLC | MagTaurate™ | View specification |
| Pyrroloquinoline quinone (PQQ) | 122628-50-6 (disodium salt) | 99% minimum by HPLC | RejuveSynergy™ | View specification |
| Trans-resveratrol (fermentation-derived) | 501-36-0 | 98% minimum by HPLC | VineGuard™ | View specification |
The full catalogue runs to 37 published ingredient specifications. Grades, salt forms and hydrate forms are quoted per order, since materials such as quercetin (anhydrous and dihydrate), trigonelline (free betaine and hydrochloride) and Rhodiola rosea extract (3% rosavins with 1% salidroside, and 5% with 2%) are supplied in more than one specification that is not interchangeable weight for weight.
We work with botanical, mineral, and cofactor-based materials, then use formulation science, analytical methods, and technical dossiers to make them easier for premium supplement brands to trust, formulate, and launch.
Format-ready ingredient support
A raw material name is not a launch plan.
Fast-growing supplement brands are building gummies, soft chews, stick packs, drink powders, liposomal liquids, beauty-from-within routines, and traceability-led capsules. The winning supplier conversation is no longer only assay and price. It is whether the ingredient can survive the format, the file review, and the claim path.
Nutrition BioTech helps buyers review the full route: ingredient fit, target format, sample path, technical file package, claim boundary, and the buyer-facing product story needed for internal approval.
Format fit
For gummies, soft chews, liquids, powders, sticks, liposomal systems, functional beverages, capsules, and tablets, the question is whether dose, taste, solubility, stability, moisture, and manufacturing route make sense for the real product.
File package
A serious review starts with COA/spec, assay or identity method, contaminant and quality notes, application boundaries, sample route, and the exact files needed by QA, R&D, sourcing, or regulatory teams.
Product story
Strong marketing does not need reckless claims. We help turn the product route into clear structure/function language, FAQ, buyer-sheet language, and red-flag claim boundaries before label or launch review.
Nature, made reviewable
Natural materials are rich. Great ingredients make them clear.
Our portfolio starts with active material identity: botanical extracts, mineral complexes, endogenous renewal concepts, and delivery-system platforms. The work is to turn that richness into a disciplined ingredient story: what it is, how it behaves, how it can be tested, and how a brand can explain it without overclaiming.
Priority platforms
Each platform connects origin, formulation behavior, and evidence.
NAD Pro
Liposomal NAD+ platform with exploratory human NAD+ elevation data and LC-MS/MS method support.
Vital Porphyrin
Coenzyme I Renewal Factor concept for methyl-burden-aware endogenous NAD+ renewal positioning.
Magnesium Acetyl Taurate
Acetyl-taurate magnesium for calm focus, evening routine, and sleep-adjacent formulation work.
Berberine Pro-Micelle Fiber 50
Botanical alkaloid platform with 50% Berberine HCl loading, dispersion data, and 1 g/day routine logic.
Natural-source matrix
Plant polyphenols, fiber carriers, lipid phases, and mineral complexes used where they improve formulation meaning.
Evidence under NDA
COA/spec, analytical notes, pilot summaries, technical bridge reports, and raw-data traceability where available.
At a glance
Four 2026 platforms with measurable points of difference.
Public claim boundary: these are ingredient development and B2B technical-review materials. Consumer-facing claims should remain structure/function oriented and undergo regulatory review.
Manufacturing and quality visuals
Nutrition Biotech quality and manufacturing environment
Real production and quality-control visuals help technical buyers understand that the ingredient story is supported by a reviewable manufacturing environment, not only marketing copy.
QC laboratory overview
quality control laboratory overview for nutraceutical ingredient testing.
Extraction equipment hall
extraction equipment hall for botanical ingredient production.
Cleanroom corridor
cleanroom corridor for controlled manufacturing access.
Batch storage area
batch storage area for nutraceutical ingredient logistics.
Start with the evidence package, not only the price quote.
Tell us which platform you are evaluating and we will provide the relevant COA, specification, sample path, technical dossier, and claim-boundary discussion.
Fast answer
What does Nutrition BioTech do?
What does Nutrition BioTech do?
Nutrition BioTech develops and supplies science-led nutraceutical ingredient platforms based on botanical actives, mineral science, cofactor biology, and delivery-system formulation support.
Buyer Q&A
Nutrition BioTech FAQ
What does Nutrition BioTech supply?
Nutrition BioTech supplies science-led nutraceutical raw materials and ingredient platforms for supplement brands, formulators, contract manufacturers, and distributors.
What makes the portfolio different from a commodity ingredient catalog?
The portfolio connects natural active identity, formulation behavior, analytical support, and B2B documentation so buyers can evaluate more than a price quote.
Which ingredient areas are currently prioritized?
Current priority areas include NAD+ platforms, endogenous renewal concepts, Magnesium Acetyl Taurate, Berberine Pro-Micelle Fiber 50, and delivery-system formulation work.
Are the materials intended for consumer disease claims?
No. Public positioning is written for structure/function supplement use and B2B technical review, not disease treatment or diagnostic claims.
What documentation can buyers request?
Buyers can request COA/spec files, formulation notes, technical bridge summaries, method support, sample availability, and relevant dossiers under NDA.
How should a brand begin evaluation?
A brand can start by identifying the target category, dosage form, claim boundary, and evidence package needed for internal review.
Technical review
Evidence Library and technical dossier pathway
Review what Nutrition BioTech can provide for B2B due diligence: COA/spec, method summaries, formulation notes, technical bridge data, pilot summaries, and sample pathway.
Formulator FAQ
Practical, claim-safe questions buyers ask about Nutrition BioTech advanced nutraceutical ingredients.
What does Nutrition BioTech do?
It works with botanical, mineral, and cofactor-based materials, then applies formulation science, analytical methods, and technical dossiers to make them easier for premium supplement brands to trust, formulate, and launch.
What does format-ready ingredient support mean?
It means supporting ingredients across the formats brands are actually building — gummies, soft chews, stick packs, drink powders, liposomal liquids, beauty-from-within routines, and traceability-led capsules — not just supplying a raw material name.
What kinds of products are these ingredients positioned for?
They are positioned for premium supplement and wellness formulas. These are market positioning categories only — the ingredients are not drugs, and Nutrition BioTech makes no disease, treatment, or cure claims.
What documentation is available for review?
On request, files can include COA and specification, identity and assay, contaminant and microbial results, and technical dossiers. The exact set depends on the material.
How does a buyer move from interest to a decision?
A buyer can explore the ingredient platforms, request samples and dossiers, and review format fit and documentation before committing to a project.
How do I request samples or dossiers?
Use the website to request samples and dossiers, noting your target format and category. The team can then share available documentation and next steps.