Public COA audit

NAD+

Audited September 5, 2026

Consistent with a legitimate COA

Document structure and test panels align with what we expect from authentic lab reports.

Legitimacy
92
Confidence
93%
Panels
5/7
Purity (printed)
99.22%

Scored high because document structure and panels look consistent with authentic lab output and broad panel coverage (5/7).

Document details

Fields extracted from the certificate — not order or payment data.

Batch / lot
CR-NAD-1000MG-2605-2
Identity method
HPLC-RTM (retention time match)
Sample date
2026-05-22
Issue date
2026-06-01

Original certificate

Embedded copy of the stored COA PDF or image. Download it for your records — PeptIQ’s audit is separate from the lab document itself.

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7-panel checklist

Had data + good, had data + bad, reported without pass/fail, or missing. Missing lowers thoroughness — you decide whether that panel matters; PeptIQ’s score still factors coverage.

5 of 7 present · 4 passed · 0 failed · 1 reported · 2 missing

Missing is a thoroughness gap — not automatically bad. PeptIQ’s legitimacy score still weighs panel coverage; you can down-weight panels that don’t matter for your use case.

  • Identity

    Tested · passed · core

    Compound identity confirmed (e.g. HPLC, mass spec).

    NAD+ Confirmed

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.22% (mean 99.15%, n=3)

  • Heavy metals

    Tested · passed

    Lead, arsenic, cadmium, mercury, or similar limits.

    All Not Detected (As, Cd, Cr, Hg, Pb)

  • Microbial

    Not on this certificate file

    Bioburden / microbial limits testing.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Endotoxin

    Tested · result on file · core

    LAL or chromogenic endotoxin assay.

    NMT 0.05 EU/mL

  • Sterility

    Tested · passed

    Sterility testing where applicable.

    No Growth

  • Residual solvent / water

    Not on this certificate file

    Residual solvents or water content limits.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

How to read this

Had data · good

Panel present with a pass (or clear acceptance).

Had data · bad

Panel present with a fail — a concrete quality signal.

Had data · unclear

Value reported without an explicit pass/fail mark.

Missing on this file

Not on this certificate file. Lowers file thoroughness; a sibling endotoxin/purity report for the same lot may still exist. PeptIQ’s score still factors coverage.

Findings

Evidence-linked observations from this audit.

  • High purity with triplicate testing

    99.22% purity (batch mean 99.15%, std dev 0.0624%) from three independent samples. This is normal for research-grade NAD+ and demonstrates rigorous QC.

  • Identity confirmed by HPLC retention time

    NAD+ confirmed by chromatographic retention time comparison with reference standard. Includes representative chromatogram.

  • Clear lot and accession numbers

    Lot CR-NAD-1000MG-2605-2, Accession ACC-2026-3014, COA COA-2026-9_RBYQ with QR code and access code KNQCYMVR.

  • Dates are consistent and valid

    Received 2026-05-22, analyzed 2026-06-01, issued 2026-06-01. All dates are on or before 2026-09-05 (today) and follow logical sequence.

  • ISO/IEC 17025 accredited lab

    ILS Laboratories, San Diego, CA. Document claims ISO/IEC 17025 accreditation. Verification URL and access code provided.

  • Comprehensive testing panel

    Full QC Panel includes purity (HPLC), identity (HPLC-RTM), heavy metals (ICP-MS), sterility (PCR), endotoxin (USP <85>), and fentanyl screen. Microbial and residual solvent panels not present.

  • Endotoxin testing present

    Endotoxin result NMT 0.05 EU/mL reported per USP <85> kinetic turbidimetric method. Document notes no universal pass/fail threshold for RUO products but states result is below commonly referenced thresholds.

  • Professional multi-page format

    3-page COA with consistent header/footer, lab logo, signature, methodology notes, and detailed results tables. Professional appearance.

PeptIQ COA reports analyze document content and publicly verifiable lab signals. They are educational and not a guarantee of product quality, legality, or safety. Always consult a qualified professional before making health decisions. We never publish purchase prices, shipping details, or uploader identity.