Quality & Traceability

The supplement industry has a quality problem, and we would rather show you our answers than ask you to trust us. Below are the questions insurers and retailers put to our manufacturer, and the plain-language answers. If you want the underlying documents for the lot you received, email us and we will send them.

Where it is made

Mega Restore is manufactured in the United States, in an FDA-registered food facility in Boca Raton, Florida, under applicable current Good Manufacturing Practice (cGMP) requirements and controlled manufacturing and quality procedures.

Where the ingredients come from

Raw materials are purchased through qualified U.S.-based suppliers. As with most nutrient supply chains, some raw materials originate outside the United States, and for those the country of origin is recorded on the applicable certificate of analysis. Supplier, manufacturer, and distributor identities are maintained in the manufacturer's purchasing, receiving, and supplier-qualification records.

Testing before anything is made

Incoming raw materials are received under quarantine and evaluated against their specifications and quality requirements before quality control releases them for use. Materials that fail are rejected and returned to the supplier. Finished product is reviewed and tested before final quality release, and a certificate of analysis is issued for each production lot.

Certificate of analysis

Current lot: the lab report for the first production lot will be posted here, with its lot number, as soon as the manufacturer releases it. Until then, the certificate of analysis for any lot is available on request.

Traceability

Every bottle carries a lot number. Every batch is manufactured under controlled batch records, which document when and where each lot was made, which raw-material lots went into it, and which suppliers those came from. Distribution records trace each lot from the manufacturer to us, and our own order records trace it from us to you. Formula and manufacturing-document changes are controlled and recorded.

If something ever goes wrong

The manufacturer maintains a formal written recall procedure, most recently revised and approved on September 1, 2026, and runs a mock recall at least once every twelve months to test that the traceability system actually works. A certificate of insurance is available on request.

How we review what we say

Product labels are reviewed by the manufacturer's quality and regulatory affairs function for applicable regulatory requirements, and the claims on this website are checked against FDA and FTC requirements. We cite the research behind our statements and note where the evidence is mixed. Dietary supplements are not intended to diagnose, treat, cure, or prevent any disease.

Questions about a specific lot, or a request for a certificate of analysis: info@functionalformulas.health.