PEPPAVITA ANALYTICAL LIBRARY

Public analytical documents.

Laboratory reports for matching launch-product specifications. Public copies are prepared to protect upstream sourcing. Submitter names, supplier-facing identifiers, upstream lot references, purchase information, and direct verification/search tokens are omitted from the customer-facing copy. Laboratory identity, test dates, methods, and analytical results are preserved.

Freedom Diagnostics

Tirzepatide

5 mg · 99.89% purity · report date 06/08/2026

View Public COA
Freedom Diagnostics

TB-500

5 mg · 99.78% purity · report date 06/08/2026

View Public COA
ILS Laboratories

GHK-Cu

50 mg · 99.65% purity · report date 08/12/2026

View Public COA
Freedom Diagnostics

CJC-1295 + Ipamorelin

5 mg + 5 mg · 99.89% purity · report date 08/04/2026

View Public COA
Freedom Diagnostics

Ipamorelin

5 mg · 99.93% purity · report date 07/18/2026

View Public COA
ALTERNATE-STRENGTH REFERENCE REPORTS

Reference reports for different strengths.

These reports document different tested strengths from the current launch SKUs. They are provided as reference documentation only and are not labeled as batch-specific COAs for the products currently offered.

ILS Laboratories · Reference

BPC-157

Reference: 10 mg · 99.81% purity · current PEPPAVITA SKU: 5 mg

View Reference COA
Freedom Diagnostics · Reference

BPC-157 + TB-500

Reference: 10 mg + 10 mg · 99.47% purity · current PEPPAVITA SKU: 5 mg + 5 mg

View Reference COA

How PEPPAVITA handles traceability

Privacy audit standard: Customer-facing analytical files must not expose supplier names, supplier contact details, supplier codes, upstream order references, submitter/customer names, or vendor-specific lot identifiers. Those records stay in PEPPAVITA's private traceability file.

Public pages use PEPPAVITA-facing product identifiers. Supplier names, supplier lot numbers, purchase records, and upstream sourcing details are maintained internally for traceability rather than published as customer-facing information.

Each laboratory report applies only to the sample submitted for analysis and should not be interpreted as proof that every vial in inventory was individually tested.