REV. 03 DEPLOYED Q1 2024 MFR: USA LOT-LEVEL TRACEABILITY DOMESTIC SHIPPING FREE OVER $60
CH.01 — Origin

Built for
operators
over 45.

The formulation originated as an internal R&D exercise by a small team of male subjects in the same cohort as the intended user. Initial intent: produce a single oral protocol that addressed observed post-45 decline without resorting to synthetic anabolics or precursor compounds.

§ 01OriginFormulation history
§ 01 — Origin Filing

22 candidate compounds. Four retained.

The candidate list was assembled from a literature scan of compounds with published human-trial evidence for endogenous testosterone support in mature male subjects. The shelf at procurement time was bracketed by two failure modes: under-dosed multivitamins relabelled as "men's wellness," and synthetic anabolic compounds with documented adverse-event literature.

Specifications were drafted against the source trials. Formulator consultations were conducted in Berlin and Dublin. The candidate list was reduced from 22 compounds to 4. Each retained compound is dosed at the level used in the source trial — not the minimum effective dose, not the marketing-claim dose.

Field deployment commenced two years into the formulation programme. The unit shipping today is the third revision of the formulation. Excipients, capsule shell, and dosing have not changed since REV. 03.

Testo Boost bottle
§ 02PrinciplesOperating constraints
§ 02 — Operating Constraints

Three constraints. Non-negotiable.

1
// CONSTRAINT

Dose to the source trial.

Each active is dosed at the level used in the trial cited as evidence of efficacy. Compounds that cannot be included at trial-level dose are excluded.

2
// CONSTRAINT

Plant-derived. No anabolics.

No synthetic hormones. No SARMs. No prohormones or precursor compounds. Botanical and mineral actives only, each with peer-reviewed evidence.

3
// CONSTRAINT

Disclose by default.

Per-lot Certificate of Analysis available on request. Sourcing origin, dose levels, and assay method are all published on the spec sheet.

§ 03ManufacturingFacility specification
§ 03 — Manufacturing

Domestic cGMP facility. Small-batch press.

Manufacturing is contracted to a small cGMP-certified facility in the United States. Batch sizes are deliberately constrained below typical contract-manufacturer minimums to maintain QA visibility and lot-level traceability through the supply chain.

FacilityGMP-certified, United States. Small-batch press.
SourcingShort, vetted list of European & Southeast Asian botanical suppliers.
Tongkat Ali originMalaysian growers, on contract with our formulator for 10+ years.
Lot QCHeavy metals, microbial contamination, active-compound content. Per lot.
CapsuleVegetarian HPMC. Lichen-derived D3. No animal-derived ingredients.
Free fromGluten, dairy, soy, nuts, GMOs, artificial colours, artificial sweeteners.
Next document

CH.03 — Formulation

Four actives. Source trials referenced. Excipients and allergen profile disclosed.

READ THE FORMULATION