Verify Quality

Professional NMN · Transparency & Documentation

Know the Source. Verify the Batch.

Novera provides full documentation for every batch. Below you'll find our key quality certificates. You can also request a copy sent directly to your inbox.

Verify your batch

Type the lot number printed on your bottle.

The lot number is printed on the bottle label. Punctuation and spacing do not matter.

What is a CoA — Certificate of Analysis Every Claim Verified — 7 Certifications, Zero Shortcuts

01 · Certificates of Analysis

Both Stages, Documented

COA

Raw Material COA — BONTAC® β-NMN

Documents the identity, 99.9% purity and tested specifications of the BONTAC® β-NMN raw material, including heavy metals and microbiological parameters.

Certificate of Analysis — Novera BONTAC NMN
COA

Finished Product COA — Current Lot

Current products available for purchase belong to finished-product lot 04.2029/NV101.

This COA verifies the finished Novera NMN 30,000 capsules, including capsule specifications, weight, microbiological results, packaging and final-product quality controls.

Finished Product COA — Novera NMN 30,000 Lot 04.2029/NV101

Click image to open the full COA in a new tab.

Two-stage verification

Novera publishes documentation for both stages of production: the BONTAC® β-NMN raw material and the finished Novera capsules. These documents use different lot numbers because they verify different stages of production.

As new production lots become available, Novera will publish the corresponding raw-material and finished-product COAs, and add each new lot to the batch lookup above, so customers can verify the documentation associated with each lot.

02 · Regulatory documentation

Origin, Manufacturing and Registration

CFS

Certificate of Free Sale

Issued by Japan's Ministry of Agriculture, Forestry and Fisheries, this document confirms that Novera NMN 30,000 may be freely sold in Japan without restriction.

Certificate of Free Sale — Novera NMN 30,000

Click image to open the public document in a new tab.

GMP

GMP Certification

GMP documentation covers the Japanese facility responsible for finished-product formulation and packaging.

GMP documentation — finished-product formulation and packaging in Japan
FDA

FDA Registration

Facility registration with the U.S. Food & Drug Administration.

FDA Registration — Novera

Request your certificate copies

Fill in your details and we'll send the full documentation package to your inbox.

We respect your privacy. Your data is used only to send the requested documentation.