OmniRayn · Supplement Labeling

The mechanism behind every claim on your label.

An audited label — and the dossier behind every line. Each claim is cited to a study your customer can open, dosed against what the human trials actually used, or reframed to what can honestly be said.

Confidential · under NDA · we confirm scope and price before any work begins.
FTC / NAD exposure cite-or-refuse every line opens a study
The exposure

A claim is only as defensible as the evidence behind it — on the day someone asks to see it.

FTC / CARSE

The substantiation standard

Every objective health-related claim needs competent and reliable scientific evidence at the studied dose.

NAD challenge

A competitor can force the question

A challenge puts your claim — and your evidence file — in front of a reviewer on a fixed timeline.

Class action

“Lack of substantiation”

Consumer-fraud suits turn a thin claim into statutory damages across every unit sold. Discovery reaches your file.

What you get

Two deliverables — an audited label, and the dossier behind it.

Each claim is weighed against the full body of human evidence — supporting and contrary — and the language is calibrated to what that evidence supports: from “Supports [X]” when the human research is strong, to “studied for [X]” when it’s emerging, to a plainly honest ingredient note when it isn’t. You get the strongest honest claim your evidence supports, with every citation open — never a dead end, never an overclaim.

“Supports” — strong human evidence “May help support” — moderate / mixed “Studied for” — emerging “Traditionally used / contains” — mechanistic
01 · THE LABEL

The label your customers read

Cited, dose-checked, honestly reframed.
A real audited supplement label produced by the engine — each claim at the strongest honest phrasing its evidence supports
02 · THE DOSSIER

The dossier behind every line

Study, dose, result, and a citation that resolves.
A real claims dossier produced by the engine — per claim: rung, mechanism, studied dose, result, and a resolving PMID

These are real documents the engine produces — click a card to open the full example (a sample product, “Calm & Recovery”). Computational / editorial work product, not legal or medical advice.

How it works

Send your claims. Get a label you can defend.

01

You send your claims + formula

Your draft label claims and ingredient list — or a finished label you want checked before it prints. Held in confidence.

02

We weigh it against the whole body of evidence

We aggregate the human trials for each ingredient and endpoint, weight them by study quality (systematic reviews over single trials), and publish where the majority of the evidence supports you — always showing the supporting and contrary studies side by side. A contrary systematic review is flagged, never buried.

03

You get the label + the dossier

An audited label and a per-claim dossier where every line resolves to a PMID / NCT / DOI — typically within 5 business days, under NDA.

Engagements

Start with a single label. Scale across your catalog.

Start here

Tear-Down

$950
one SKU · ~48 hours
  • Your top-selling SKU run through the engine
  • Every claim graded, with a dose-adequacy flag (label dose vs. studied range)
  • The gaps a challenger would target — cited
  • Credited toward a full label + dossier
Request a tear-down

Single label

$3,900
one-time · one product / SKU
  • The audited label + full per-claim dossier
  • Each claim cited, dose-checked, or reframed
  • Non-listed actives named by compound
  • Every published claim cited or refused — resolving PMID / NCT / DOI
  • Counsel-ready review pack — a memo your attorney signs off in ~1 hour, not 20
  • Covers up to ~6 actives / 10 claims — larger formulas scoped first
  • Under NDA, ~5 business days
Request a review

White-label / CMO

Contact
portfolio · manufacturer · privileged
  • Bulk or portfolio-wide auditing
  • White-label / contract-manufacturer output
  • Counsel-directed, privileged engagements
Talk to us
01 · SubmitYou send claims + formula, in confidence.
02 · NDA + scopeWe reply within 1 business day with an NDA, scope, and a secure payment link.
03 · AuditOn payment, we deliver the label + dossier in ~5 business days.

Outputs are informational work product, prepared for review at the direction of counsel — not legal advice. Studied ranges are cited facts, not a dose recommendation. You approve scope and price before any charge — nothing is billed on submission.

Request a labeling review.

Tell us the claim and the ingredient. We’ll show you what the human literature supports, at what dose — and what it can’t. Confidential, and binding on nothing.

Request a review
Under NDA · we confirm scope and price before any work · from $950 for a Tear-Down, $3,900 for a full label + dossier.