ACR Aavant
Vials tend to hold more than the label (median +9.4%); 0 of 41 vials were more than 10% under.
For research use only. VendorVerify sells nothing and takes no money from vendors. No affiliate links, no coupon codes, no paid rankings. How scores work
Every vial we have on file
- Within ±5% / purity 99%+
- 5–20% under, overfilled / purity 95–99%
- Failed: over 20% under, over 50% over, empty or under 95% pure
Dose vs label
41 vials measured · 0 emptyPurity
45 vials measured- Median purity
- 99.68%
- across 45 vials
- Median dose vs label
- +9.4%
- across 41 vials; + means more than the label
- Failed vials
- 0.0%
- 0 of 45 vials; the rate weights each lab report equally and recent reports more, as the score does
- Lab reports
- 17
- Mar 14, 2025 to Feb 16, 2026
Labs: Janoshik, Peptide Test
Key facts
- VendorVerify holds third-party lab results for 45 ACR vials from 17 lab reports, dated Mar 2025 to Feb 2026.
- 1 of those ACR lab reports was commissioned by ACR itself and count at half weight in the score.
- 0 of 45 ACR vials failed: empty, under 95% pure, more than 20% under the label or more than 50% over it.
- The median ACR vial tested at 99.68% purity across 45 vials with a purity result.
- The median ACR vial held +9.4% compared with its label across 41 vials where the lab measured the amount.
- Buyers have had 3 different compounds from ACR lab tested.
- ACR ranks #5 of 30 ranked vendors on the VendorVerify score.
- ACR vials on file were tested by Janoshik, Peptide Test.
By peptide
| Peptide | Vials | Failed | Median purity | Median dose vs label | Dose vs label, −20% to +20% |
|---|---|---|---|---|---|
| Tirzepatide | 28 | 0 | 99.68% | +9.6% | |
| Retatrutide | 12 | 0 | 99.69% | +7.0% | |
| KPV | 5 | 0 | 98.90% | +5.6% |
Lab reports
One row per tested vial, newest first. Tests marked vendor-commissioned were paid for by ACR; they count at half weight in the score and don't count toward ranking.
| Date | Peptide | Lab | Label | Measured | Dose vs label | Purity |
|---|---|---|---|---|---|---|
| Feb 16, 2026 | RetatrutideBatch 967286-000004 (vendor inferred from batch code; report lists manufacturer as Unknown) | Janoshik | 12 mg | 13.51 mg | +12.6% | 99.15% |
| Feb 16, 2026 | RetatrutideBatch 967286-000004 (vendor inferred from batch code; report lists manufacturer as Unknown) | Janoshik | 12 mg | 13.59 mg | +13.2% | 99.18% |
| Feb 16, 2026 | RetatrutideBatch 967286-000004 (vendor inferred from batch code; report lists manufacturer as Unknown) | Janoshik | 12 mg | 13.52 mg | +12.7% | 99.13% |
| Jan 23, 2026 | TirzepatideBatch 967288-000002 | Janoshik | 60 mg | 58.21 mg | −3.0% | 99.91% |
| Jan 5, 2026 | KPVBatch 967289-00001 (Clear lavendar cap) | Janoshik | 15 mg | 15.56 mg | +3.7% | 98.85% |
| Jan 5, 2026 | KPVBatch 967289-00001 (Clear lavendar cap) | Janoshik | 15 mg | 15.84 mg | +5.6% | 98.90% |
| Jan 5, 2026 | KPVBatch 967289-00001 (Clear lavendar cap) | Janoshik | 15 mg | 15.44 mg | +2.9% | 98.61% |
| Dec 23, 2025 | RetatrutideBatch r11 Batch 3 | Janoshik | — | 10.66 mg | — | 99.69% |
| Nov 24, 2025 | KPVBatch 967289-000001 (purple cap)Vendor-commissioned | Janoshik | 15 mg | 17 mg | +13.3% | 99.68% |
| Nov 24, 2025 | KPVBatch 967289-000001 (purple cap)Vendor-commissioned | Janoshik | 15 mg | 17.11 mg | +14.1% | 99.75% |
Other lab tests
Endotoxin, TFA, counterion and contaminant checks, as reported by the lab. They are shown for transparency and are not part of the score.
| Date | Peptide | Test | Result | Lab |
|---|---|---|---|---|
| Feb 24, 2026 | RetatrutideBatch 967286-000004 (vendor inferred from batch code; report lists manufacturer as Unknown) | Sterility | TAMC=Pass, TYMC=Pass | Janoshik |
| Feb 16, 2026 | RetatrutideBatch 967286-000004 (vendor inferred from batch code; report lists manufacturer as Unknown) | LCMS | Mannitol, retatrutide, and degradation products; no significant contamination | Janoshik |
| Feb 13, 2026 | RetatrutideBatch 967286-000004 (vendor inferred from batch code; report lists manufacturer as Unknown) | Endotoxin | <10 EU/Vial (1.641 EU/Vial estimate) | Janoshik |
| Feb 6, 2026 | TirzepatideBatch 967288-000002 | Sterility | TAMC=Pass, TYMC=Pass | Janoshik |
| Jan 30, 2026 | KPVBatch 967289-0001 | Sterility | TAMC=Pass, TYMC=Pass | Janoshik |
| Jan 29, 2026 | TirzepatideBatch 967288-000002 | Heavy Metals | Not detected (As, Cd, Pb) | Janoshik |
| Jan 26, 2026 | TirzepatideBatch 967288-000002 | Endotoxin | >10 EU/Vial (15.135 EU/Vial estimate) | Janoshik |
| Jan 26, 2026 | TirzepatideBatch 967288-000002 | TFA | Not detected | Janoshik |
| Jan 22, 2026 | TirzepatideBatch 967288-000002 | LCMS | Mannitol, tirzepatide, and degradation products | Janoshik |
| Jan 20, 2026 | RetatrutideBatch 967285-000005 | Sterility | TAMC=Pass, TYMC=Pass | Janoshik |
ACR: common questions
Is ACR legit?
We can't vouch for any vendor as a business, and we don't sell or recommend products. What we can show is what buyers' independent lab tests found: 0 of 45 ACR vials on file failed, meaning they were empty, under 95% pure, more than 20% under the label or more than 50% over it. That places ACR #5 of 30 ranked vendors, above market on our score. Results on file run from Mar 2025 to Feb 2026.
Has ACR been third-party tested?
Yes. We hold results for 45 ACR vials from 17 lab reports, tested by Janoshik, Peptide Test. 16 of those reports were paid for by buyers or group tests; 1 was commissioned by ACR itself, verified at the lab, and count at half weight in the score.
Are ACR vials dosed correctly?
Across 41 vials where the lab measured the amount, the median ACR vial held +9.4% compared with its label. 0 of 41 held more than 10% less than the label said.
How pure is ACR?
The median ACR vial tested at 99.68% purity across 45 vials with a purity result. We count anything under 95% as a failed vial, and a vial at 99.5% or higher gets full marks for purity.
Does ACR pay to be listed or ranked?
No. VendorVerify sells nothing and takes no money from vendors. No affiliate links, no coupon codes, no paid rankings. A vendor's place comes only from lab results.
Will my ACR vial match these results?
Not necessarily. A lab report describes the vials that were tested, and batches differ. A clean record lowers the odds of a bad vial but doesn't rule one out, which is why newer reports count for more in the score.
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