How every MemoHoney lot is made and tested
MemoHoney is manufactured in the United States in an FDA-registered facility operating to cGMP standards. Each finished lot is sampled and screened by Aldermere Assay Group, LLC, an independent laboratory working under ISO/IEC 17025 accreditation, before any of it is released for distribution.
What runs on every lot
| Test | Method | Result on the current run |
|---|---|---|
| Identity | UHPLC-MS fingerprint against a reference standard | Confirms each named ingredient is the compound it claims to be. |
| Active purity | UHPLC-MS, chromatographic | Current run returned 99.3%. |
| Heavy metals | ICP-MS for lead, arsenic, cadmium and mercury | Current run returned < 0.35 ppm (ICP-MS). |
| Microbiology | Total plate count, yeast and mould, pathogen screen | Current run: Within USP <2021> limits. |
| Allergen screen | Dairy and gluten protein assay | Not detected. The capsule shell is hypromellose. |
| Non-GMO status | Supplier documentation with identity preservation | All amino acid material is fermentation-derived. |
The numbers on the current run are published on the batch verification page with the certificate number. This page describes the procedure; that page carries the result.
What the certifications actually mean
FDA-registered facility
The manufacturing site is registered with the Food and Drug Administration, which means it is on file with the agency and subject to inspection. It does not mean the FDA has approved the product. The agency does not approve dietary supplements at all, and any brand implying otherwise is misleading you.
cGMP
Current Good Manufacturing Practice is the framework covering how a facility documents, controls and verifies what it produces: written procedures, batch records, equipment qualification, staff training and retained samples. It is about process control rather than proof of effect.
ISO/IEC 17025
This is the accreditation that applies to a testing laboratory rather than a factory. It covers method validation, equipment calibration, competence of the analysts and traceability of results. It is the reason an outside laboratory result carries more weight than an in-house one.
Retained samples
A sealed sample of each lot is kept for the shelf life of the product plus one year, which is what allows a lot to be re-examined later if a question arises about it. Without retained samples, a certificate is a snapshot nobody can revisit.
What testing does not tell you
A certificate of analysis answers three questions: is each ingredient what it says it is, is it present at the purity claimed, and is the lot free of contamination above set limits. Those are worth knowing and they are not the same as evidence that the finished product works.
Two further limits are worth stating plainly. Testing cannot confirm milligram amounts against a label that does not print any, so the missing dosage column on the ingredient panel is not something a laboratory result can fix. And screening says nothing about how a formula behaves in a person, which is a question for clinical research rather than chromatography.
The desk publishes what it has. Where the record is silent, the page says so.
Written for general education. It is not a substitute for advice from your own clinician, so speak with a pharmacist or physician before adding any supplement, particularly if you take blood pressure medication, nitrates or erectile dysfunction drugs.
Documented lot, published certificate, sixty-day guarantee
Testing is the part Larkmont can control and publish. The guarantee covers the part it cannot, which is whether the formula does anything for you specifically.
- 60-day money-back guarantee
- Authorized 2026 distribution
- FDA-registered facility
- cGMP manufacturing
- Batch MH-26/A-0417 on record