At a glance
Product details
- +10 mg strength per vial
- +Ten-vial research kit
- +Product identifier TSM10
HUMAN+Tesamorelin10mg/vialTSM10
HUMAN+Tesamorelin10mg/vial
Peptides
Tesamorelin (TSM10)
Tesamorelin (TSM10) is the 10 mg presentation in the HUMAN+ peptide catalog. This page brings its kit format, identifier, price, and verification guidance together so the essentials are easy to review before ordering.
$500.00USD · availability shown at checkout
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Package record
What to verify
- Catalog code
- TSM10
- Format
- 10mg/vial, 10 vial/kit
- Collection
- Peptides
- Presentation
- HUMAN+ labeled vial and carton
Care & handling
Before opening
- Keep the product sealed and follow the storage directions supplied with the item.
- Confirm the name, strength, code, and lot information match the accompanying record.
- Review available documentation before use and contact support if anything is unclear.
US / THEM · The documentation difference
Evidence over
empty claims.
A clean label is only the beginning. The HUMAN+ standard is built around product identity, lot-level traceability, inspectable source records, and measured reporting.
H+
HUMAN+ verification standardDesigned to be traceable.
| What to compare | H+ HUMAN+ standard | Typical unverified listing |
|---|---|---|
| Product identity | ✓ Tesamorelin (TSM10), TSM10, and 10mg/vial, 10 vial/kit are presented together in one product record. | — A generic title with missing, incomplete, or inconsistent identifiers. |
| Lot traceability | ✓ A lot-matched record is required before verified status should appear on a product. | — No clear connection between the item being sold and the report being shown. |
| Certificate access | ✓ The original independent COA should remain complete, downloadable, and open to inspection. | — A cropped screenshot, marketing summary, or no source document at all. |
| Measured reporting | ✓ Identity and purity values should come directly from the reviewed analytical report. | — Vague “premium” or “high purity” language without measured evidence. |
| Source transparency | ✓ The issuing laboratory or verified manufacturing source should be named on the record. | — Testing source, report date, methods, or responsible party are not disclosed. |
| Accountability | ✓ Product-specific information, a clear support path, and evidence-before-claims review. | — An anonymous listing with unclear ownership, documentation, or follow-up support. |