Vial Guide

Testing and fakes

What independent tests of peptide products have found, what a test can and can’t tell you, and the claims to read carefully. No sellers or testing labs are named here.

What tests of real products found

Published analyses of products bought online or seized, and what regulators found in the paperwork sent to them.

ProductTestedWhat they foundSource
Semaglutide from illegal online pharmacies6 orders3 prefilled pens never arrived. The 3 vials that did held 29 to 39% more semaglutide than labeled, all carried bacterial toxins (endotoxin), and purity measured 8 to 14% against the 99% claimed.Ashraf et al., J Med Internet Res 2024
Products sold as SARMs44 products (2016)Only 23 contained a SARM. 17 held other unapproved drugs, including MK-677, 4 held no active drug, 11 had ingredients not on the label, and the amount matched the label in 18.Van Wagoner et al., JAMA 2017
Melanotan 2Vials from 3 online shopsLabeled 10 mg, the vials held 4.3 to 8.8 mg; two shops’ vials had 4.1 to 5.9% unknown impurities.Breindahl et al., Drug Test Anal 2015
TB-500 and related products3 productsTB-500 products didn’t consistently match their own descriptions, and one product sold as a growth factor was mostly sheep tissue and blood proteins.Delcourt et al., Drug Test Anal 2023
Growth hormone and GHRP powdersSeized black-market productsA growth hormone with an extra amino acid, and glycine-extended versions of GHRP-2, GHRP-6 and ipamorelin: variants whose effects in people are unknown.Krug et al., Growth Horm IGF Res 2018
Custom research peptides2 peptides from a commercial supplier20% and 43% of each sample’s weight was mannitol, a sugar alcohol nobody declared. The usual purity test, HPLC with UV detection, can’t see it; NMR found it.Choules et al., J Pharm Biomed Anal 2020
Glutathione injectionsAn outbreak, 2026Injections compounded from supplement-grade powder caused reactions to bacterial toxins, including low blood pressure and shock, in more than 25 people in at least 4 states.CDC, September 2026
Certificates of analysis sent to FDAPeptides nominated for compounding (2024–2026)For peptides such as BPC-157, MOTS-c and CJC-1295 (no DAC), certificates lacked tests for impurities, microbes or endotoxins; some listed purity alone.FDA advisory committee briefings

What a test can and can’t show

TestShowsCan’t show
Mass spectrometryThat the molecule has the right mass, so it’s probably the right peptideHow much is there, or whether it’s sterile
HPLC purityWhat share of the peptide-like material, by UV signal, is the target peptideSalt, water and fillers such as mannitol, so not how much peptide the vial holds
Assay (content)How many milligrams of peptide the vial actually holdsImpurities or contamination
EndotoxinFragments of bacteria that cause fever and inflammationWhether live microbes are present
SterilityWhether live microbes grow from the sampleEndotoxin, which can be present in a sterile product

Every result describes one sample from one lot, on the day it was tested. Reading a lab report explains each test in more detail.

Claims to read carefully

“99% pure”

Usually an HPLC number. It describes the peptide-like material, not how much peptide is in the vial, and it can miss salt, water and fillers entirely, as the mannitol case shows.

“Third-party tested”

Ask which lot was tested, by whom, for what, and when. A certificate that lacks a lot number matching your vial, or covers identity and purity only, leaves out most of what matters for an injection.

“Research use only”

No regulator checks these products. In 2026, FDA rejected the disclaimer in warning letters where sellers’ websites showed the products were meant for people, and Australia’s TGA says it doesn’t make importing them lawful.

Brand names on powder vials

No approved semaglutide or tirzepatide product is a powder to mix: the approved forms are ready-made solutions and tablets, dispensed by licensed pharmacies on a prescription. FDA is aware of counterfeit Ozempic in the US market.

Sources: Ashraf et al., J Med Internet Res 2024, PMID 39509151; Van Wagoner et al., JAMA 2017, PMID 29183075; Breindahl et al., Drug Test Anal 2015, PMID 24771717; Delcourt et al., Drug Test Anal 2023, PMID 36482504; Krug et al., Growth Horm IGF Res 2018, PMID 29864719; Choules et al., J Pharm Biomed Anal 2020, PMID 31671336; CDC, adverse events linked to injectable glutathione (September 2026); FDA Pharmacy Compounding Advisory Committee briefing documents (2024–2026); FDA warning letters to online sellers (March 31, 2026); FDA, concerns with unapproved GLP-1 drugs used for weight loss; TGA, responsibilities when importing unapproved peptide products (checked October 2026).