Ubiquinol Laboratory Results — Lot 261005
Quality / Public Verification View
Independent laboratory results for Ubiquinol.
- Laboratory
- Bis Laboratories
- Report number
- 2610026-1
- Report date
- October 22, 2026
- Product
- Ubiquinol
- NPN recorded on report
- 80139357
- Lot
- 261005
Download laboratory results (PDF summary) ↗
The downloadable public summary is prepared by DR.MORGAN from the named independent laboratory report. It is not the original laboratory-issued certificate.
Results and report limits
Each result below is transcribed from the identified report. “<” means the reported result is below the stated reporting threshold. Heavy-metal results are expressed in micrograms per kilogram body weight per day (µg/kg b.w./day), using the report’s 70 kg adult body-weight assumption and one-capsule-per-day calculation. This calculation is a laboratory exposure basis, not an instruction for use.
- Arsenic
- Result: < 0.00078 µg/kg b.w./day. Report limit: < 0.14 µg/kg b.w./day. Method: USP <233>.
- Cadmium
- Result: < 0.00003 µg/kg b.w./day. Report limit: < 0.09 µg/kg b.w./day. Method: USP <233>.
- Lead
- Result: < 0.00037 µg/kg b.w./day. Report limit: < 0.14 µg/kg b.w./day. Method: USP <233>.
- Total mercury
- Result: < 0.00017 µg/kg b.w./day. Report limit: < 0.29 µg/kg b.w./day. Method: USP <233>.
- Total aerobic microbial count (TAMC)
- Result: < 10 CFU/g. Report limit: < 1000 CFU/g. Method: USP <2021>.
- Total yeast and mould count (TYMC)
- Result: < 10 CFU/g. Report limit: < 100 CFU/g. Method: USP <2021>.
- Salmonella spp.
- Result: Absent. Report limit: Absent in 10 g. Method: USP <2022>.
- Escherichia coli
- Result: Absent. Report limit: Absent in 10 g. Method: USP <2022>.
- Staphylococcus aureus
- Result: Absent. Report limit: Absent in 10 g. Method: USP <2022>.
Heavy-metal limits are identified in the report as based on Health Canada’s Quality of Natural Health Products Guide. Microbiological limits are identified as based on USP <2023>.
Scope and limitations
These results apply only to the sample and lot identified in this report. They do not establish clinical efficacy, confirm every ingredient amount, or demonstrate results for every production batch. This page does not identify the lot currently being shipped. Follow the current product label and licensed information for use.
This public verification view presents relevant testing information without distributing the original report. Recipient details, private contact information and approval signatures are omitted.
Batch-specific manufacturing and quality documentation is available upon request and is reviewed manually by DR.MORGAN.
