Certificate of Analysis
KLOW Blend
Batch Report on File
>99.9%Purity
ProductKLOW Blend
VariantKLOW Blend 50mg + 10mg + 10mg + 10mg
Lot / Batch #PV-2608-KLOW-01
LabeledGHK-Cu 50mg + KPV 10mg + BPC-157 10mg + Thymosin Beta-4 10mg
ActualBPC-157 9.78mg · GHK-Cu 48.8mg · KPV 10.8mg · Thymosin Beta-4 9.29mg
TestedSeptember 8, 2026
Analytical Results
Chromatographic Purity · HPLC-UV/MS >99.9%
BPC-157 · 10mg label · HPLC-UV/MS · ID confirmed 9.78mg · 97.8% of label
GHK-Cu · 50mg label · HPLC-UV/MS · ID confirmed 48.8mg · 97.6% of label
KPV · 10mg label · HPLC-UV/MS · ID confirmed 10.8mg · 108.0% of label
Thymosin Beta-4 · 10mg label · HPLC-UV/MS · ID confirmed 9.29mg · 92.9% of label
Endotoxins · USP 85 · LAL clot <0.5 EU
Elemental Impurities · USP 233 · As/Cd/Hg + duplicate Hg row on report ND on all reported analytes
Performing Laboratory
Independent third-party laboratory
Independent third-party laboratory · USP / compendial testing standards
Disclaimer & Scope of Testing
For research use only. Not for human or veterinary consumption, and not for diagnostic, therapeutic, or clinical use. The product analyzed has not been evaluated by the U.S. Food and Drug Administration.
Testing is performed by an independent, third-party laboratory using the methods identified on the applicable report. Results apply only to the specific sample and lot identified above. Test results reflect the sample as received; subsequent handling, storage, or modification may alter the attributes reported here. The laboratory report is the controlling source for analytical methods, results, limits, and any acceptance criteria.