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Demonstration Record
Analytical values shown in this experience are illustrative sample data for portal demonstration purposes only.
Nuform Ipamorelin
NF
Nuform Labs
Nuform Ipamorelin
Lyophilized 5mg Vial
Lot
LOT-4-0243
Batch
B-1016
Released
June 11, 2026
EA Sample
ETH-01016
Brand submitted sample
Supplied by the brand, not bought by TrueView
Accredited Lab Testing
ISO/IEC 17025 lab, sample chosen by the brand
Results Available
Report published
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Quantitation
Ipamorelin
97.2
%
of label claim
Label claim:
5.00
mg
· Detected:
4.86
mg
Detected
4.86
mg
Label claim
5.00
mg
0%
97.2
%
Label claim achieved
Purity
98.6
%
Tests Passed
7
/
7
Overall
Passed
Identity
Confirmed
Peptide identity
Method:
USP <621>
Specification:
Matches reference standard
Confirmed
Confirmed
Purity
Passed
Chromatographic Purity
Method:
HPLC
Specification:
≥ 98.5%
98.6
Pass
Quantity / Quantitation
1 analyte verified
Quantitation
Ipamorelin
97.2
%
of label claim
Label claim:
5.00
mg
· Detected:
4.86
mg
Detected
4.86
mg
Label claim
5.00
mg
0%
97.2
%
Label claim achieved
Bacterial Endotoxins
Passed
Bacterial Endotoxins
Method:
Gel-clot LAL (USP <85>)
Specification:
≤ 10 EU/mg
0.5 EU/mg
Pass
Residual Solvents
Passed
Residual solvents (GC)
Method:
USP <467>
Specification:
≤ ICH Q3C limits
< LOD ppm
Pass
Heavy Metals
4/4 passed
Arsenic (As)
4.7%
0.07 mcg/g
1.5 mcg/g
Cadmium (Cd)
4.7%
0.07 mcg/g
0.5 mcg/g
Lead (Pb)
4.7%
0.12 mcg/g
1 mcg/g
Mercury (Hg)
4.7%
0.07 mcg/g
1.5 mcg/g
[{"analyte":"Arsenic (As)","result":"0.154 mcg/g","limit":"≤ 1.5 mcg/g","status":"pass"},{"analyte":"Cadmium (Cd)","result":"0.085 mcg/g","limit":"≤ 0.5 mcg/g","status":"pass"},{"analyte":"Lead (Pb)","result":"0.232 mcg/g","limit":"≤ 1.0 mcg/g","status":"pass"},{"analyte":"Mercury (Hg)","result":"0.120 mcg/g","limit":"≤ 1.5 mcg/g","status":"pass"}]
Microbiology
Passed
Microbiological analysis
Method:
USP <61> / <62>
1/1 Passed
Pass
Sterility
Passed
Rapid sterility
Method:
Rapid sterility qPCR (USP <1223>)
Specification:
No growth at 14 days
Pass
Pass
Fentanyl
Passed
Fentanyl screen
Method:
Specification:
Not Tested
Pass
Ethos Analytics
Certificate of Analysis
Original Laboratory Report
SAMPLE REPORT — For demonstration only
Ethos Analytics
Independent analytical laboratory, Phoenix Arizona
Phoenix, AZ
ISO/IEC 17025
EA Sample ID
ETH-01016
Batch / Lot
LOT-4-0243
Date Received
June 2, 2026
Date Completed
June 11, 2026
Standard
ISO/IEC 17025:2017
Laboratory
Ethos Analytics
Phoenix, AZ
Analysis Summary
Identity
USP <621>
Pass
Purity
HPLC
Pass
Quantity
HPLC
Pass
Endotoxin
Gel-clot LAL (USP <85>)
Pass
Residual Solvents
USP <467>
Pass
Heavy Metals
ICP-MS (USP <233>)
Pass
Microbiology
USP <61> / <62>
Pass
Sterility
Rapid sterility qPCR (USP <1223>)
Pass
Fentanyl
USP <2251>
Pass
View Original Ethos CoA
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