Lutemax 2020
marigold-derived lutein and zeaxanthin isomers
LuteinLast reviewed: July 11, 2026
Medical & Industry Advisor: Dr. James Pendleton, ND
Answer
Availability
We have not verified a current supply status for this ingredient. Unknown is our default: we publish a status only with dated evidence. If you have first-hand sourcing information, use the correction link below.
Owner and access
- Access model
- Licensed program
What it is
- Marigold-extract lutein/zeaxanthin ingredient described by OmniActive as IP-protected. [omniactives.com]
Spec parameters buyers should demand
What to ask for on the certificate of analysis and spec sheet. Identity, quality, and regulatory parameters only. This is not advice about efficacy.
| Parameter | What to ask | Why it matters |
|---|---|---|
| Carotenoid content and isomer profile | Request the certificate of analysis stating total carotenoid content, lutein content, and the ratio of lutein to zeaxanthin isomers. OmniActive publishes Lutemax 2020 as carrying the three macular carotenoids (lutein, RR-zeaxanthin, and RS/meso-zeaxanthin) in a 5:1 lutein-to-zeaxanthin-isomer ratio.[omniactives.com — Lutemax 2020][USP Lutein Reference Standard] | Carotenoid products vary widely in isomer content, so the assay and the isomer ratio are what tell you which material you actually have. |
| Identity verification | Confirm the manufacturer runs at least one validated identity test on each incoming lot (for example HPLC), as 21 CFR 111.75(a)(1) requires for every dietary ingredient.[21 CFR 111.75(a)(1) — identity test required for each dietary ingredient] | Identity testing is a federal manufacturing requirement, and a certificate that names the method is the record your own quality file needs. |
| Botanical origin | Ask the CoA to confirm the marigold (Tagetes erecta) origin of the carotenoids and the extraction/saponification basis, and request the residual-solvent results.[USP Lutein Reference Standard] | Marigold-derived macular carotenoids are the specified material; documented origin and residual-solvent control confirm the extract matches the specification. |
| Heavy metals | Request lead, arsenic, cadmium, and mercury results with the test method and the limits applied.[21 CFR Part 111 — cGMP for dietary supplements] | Heavy-metal control is a baseline quality attribute for any botanical extract and part of a complete certificate of analysis under 21 CFR Part 111. |
QC and testing considerations
- Every dietary ingredient must pass at least one validated identity test before use (21 CFR 111.75(a)(1)). Confirm your manufacturer runs identity testing on each incoming lot. [21 CFR 111.75(a)(1)]
- 'Lutein/zeaxanthin' materials differ in their isomer breakdown; ask the CoA to report lutein, RR-zeaxanthin, and meso-zeaxanthin separately rather than a single combined figure so the material matches the specification you intend. [omniactives.com — Lutemax 2020]
- Marigold carotenoids are light- and oxygen-sensitive; ask about the delivery matrix (beadlet, oil, or powder) and stability data, and request the residual-solvent results from the extraction. [USP Lutein Reference Standard]
Further reading: How to read a certificate of analysis and third-party supplement testing.
Reference list
- USP Lutein Reference Standard (compendial identity/assay standard) Pharmacopeia
- 21 CFR Part 111 — Current Good Manufacturing Practice for dietary supplements (identity testing at 111.75) Regulatory
- Lutemax 2020 (OmniActive Health Technologies) — branded lutein/zeaxanthin, owner site Owner technical
A reference list is not claim substantiation. Under the FTC's Health Products Compliance Guidance (December 2022), marketing claims about a finished product require competent and reliable scientific evidence, typically randomized, controlled human clinical testing. Responsibility for substantiating product claims rests with the brand.
Manufacturers with stated capability
No manufacturer has a listed capability for this ingredient yet. Listings are positive-only: an entry states a manufacturer can run the ingredient, never that one cannot.
Run this ingredient? Request inclusion.
Further reading
The decision framework behind this reference: five checkable criteria for choosing between a branded ingredient and its generic form.
What this page does not tell you
- Whether the owner will license your specific product or accept a new account.
- Pricing, minimum order volumes, or contract terms.
- Anything about efficacy. This is an identity and sourcing reference.
Prefills the ingredient into the RFQ Spec Builder. You enter your own formula; the tool formats it into a spec sheet.
Lutemax 2020 is a branded ingredient of OmniActive Health Technologies. Inventory Ready is not affiliated with, licensed by, or endorsed by OmniActive Health Technologies.
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