PEL Report Guide · September 15, 2026
Wolverine Stack report: BPCTB014 | Pacific Edge Labs
Read the Freedom Diagnostics source for BPC-157 10mg TB500 10mg, lot BPCTB014: 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 | BPC-157 10mg TB500 10mg |
| Lot printed on original | BPCTB014 |
| Report date | 2026-06-15 |
| Report/accession identifier | 2606120125 |
| 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) | TB-500 / BPC-157 |
| Purity (HPLC-UV), analytical-results row | 99.80% |
| Net content average, as printed | TB-500: 5.06 mg; BPC-157: 6.11 mg |
| Individual vial purity / content | Vial 1: 99.85%; TB-500 5.33 mg, BPC-157 6.24 mg. Vial 2: 99.74%; TB-500 4.79 mg, BPC-157 5.97 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
Document discrepancy to resolve: the product heading says BPC-157 10mg TB500 10mg, while the net-content averages state TB-500 5.06 mg and BPC-157 6.11 mg. These values are reproduced without correction. This page does not establish why they differ or whether BPCTB014 is currently supplied. Ask PEL to reconcile the selected option, supplied lot and original laboratory report before relying on a 10 mg + 10 mg match.
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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