PEL Report Guide · September 15, 2026
GLOW report: GLOW017 | Pacific Edge Labs
Read the Freedom Diagnostics source for GLOW 70mg, lot GLOW017: sample identifiers, methods, reported measurements and the original document.
Publisher: Pacific Edge Labs. This is a factual reading of a displayed original report, checked on September 15, 2026. It is not a new laboratory test or a certification of current stock.
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Document identity
| Laboratory named on original | Freedom Diagnostics |
|---|---|
| Client named on original | Pacific Edge Labs |
| Sample/product label | GLOW 70mg |
| Lot printed on original | GLOW017 |
| Report date | 2026-06-15 |
| Report/accession identifier | 2606120173 |
| Received date | 2026-06-12 |
Measurements stated in the source
Values below are transcribed from the original; no result is recalculated or substituted. Percent purity and measured quantity are different fields.
| Field / method as stated | Result in original |
|---|---|
| Identity (LC-MS) | GHK-Cu / Thymosin Beta-4 / BPC-157 |
| Purity (HPLC-UV), analytical-results row | 99.59% |
| Net content average, as printed | GHK-Cu: 56.56 mg; Thymosin Beta-4: 9.96 mg; BPC-157: 9.23 mg |
| Individual vial purity / content | Vial 1: 99.55%; GHK-Cu 55.99 mg, Thymosin Beta-4 9.61 mg, BPC-157 8.69 mg. Vial 2: 99.62%; GHK-Cu 57.14 mg, Thymosin Beta-4 10.32 mg, BPC-157 9.77 mg. |
| Endotoxin replicates 1 and 2 | Both marked Pass; source states LAL assay, USP <85>, assay sensitivity ≤0.05 EU/mL. |
| Microbial analysis (PCR) | Source states no detectable microbial DNA and marks Pass; its stated assay targets common microbial contaminants. |
How to use this record
The source reports component measurements, not just a total blend weight. Keep these measured averages distinct from labelled component amounts. This GLOW document is not evidence for the separate KLOW blend or a KPV component.
Match the selected product, amount and physical supplied lot to the original document before relying on it. A report does not establish the condition of every vial or a future lot. Testing method names and laboratory statements are attributed to the source, not independently audited here. No human-use or sterility conclusion is made.
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