PeakFusion Supplements

Lab Results & Certificates of Analysis

Every PeakFusion product is independently tested by an accredited laboratory in compliance with current Good Manufacturing Practices (cGMP). The results below are tied to specific production lot numbers and reflect the current product in circulation.

These are not marketing claims. These are the verified test results for your product.

Product 1 of 3

Micronized Creatine Monohydrate

Lot B25I013  ·  Manufactured September 2025  ·  Tested March 4, 2026

Test Specification Result Method
Appearance White Powder ✓ Complies Visual
Identification Complies by TLC ✓ Complies TLC
Assay (Purity) 99.9% Minimum 100.8% Liquid Chromatogram
Lead 1 PPM Maximum ✓ Conforms USP 251
Arsenic 1 PPM Maximum ✓ Conforms USP 211
Cadmium 1 PPM Maximum ✓ Conforms AAS
Total Plate Count <10 cfu/g ✓ Pass USP <2021>
Yeast & Mold <10 cfu/g ✓ Pass USP <61>
E. coli Absent ✓ Absent USP <61>
Salmonella Absent ✓ Absent USP <61>
Staphylococcus aureus Absent ✓ Absent USP <61>
Pseudomonas aeruginosa Negative / 10g ✓ Negative USP <2022>
Summary: Lot B25I013 passed all physical, identity, purity, heavy metals, and microbiological tests. Assay result of 100.8% exceeds the 99.9% minimum specification, confirming full-potency creatine monohydrate with no detectable pathogens or heavy metal exceedances.

Product 2 of 3

Vitamin D3 2,000 IU

Lot VS220698  ·  Manufactured December 2022  ·  Tested February 11, 2026

Test Specification Result Method
Average Fill Weight 151 mg (±10%) 139.25 mg ✓ CSI-QC-GT-102
Disintegration NMT 30 minutes 7 minutes USP <2040>
Appearance Clear size 3 oval softgel, clear yellow fill ✓ Conforms Organoleptic
Vitamin D3 (Cholecalciferol) 50 mcg (2,000 IU) — ≥100% of label 56.4 mcg (2,556 IU) UPLC
Total Plate Count NMT 3,000 cfu/g <100 cfu/g ✓ AOAC
Yeast and Mold NMT 300 cfu/g <100 cfu/g ✓ AOAC
E. coli Absent ✓ Absent AOAC
Salmonella species Absent ✓ Absent USP <2022>
Staphylococcus aureus Absent ✓ Absent AOAC
Summary: Lot VS220698 passed all physical, quantitative, and microbiological tests. The measured dose of 2,556 IU per softgel exceeds the 2,000 IU label claim by approximately 28%. Disintegration completed in 7 minutes against a 30-minute maximum. All microbiological tests absent or below detection limits.

Product 3 of 3

Complete Multivitamin

Lot MMV250805  ·  Manufactured May 8, 2025  ·  Tested September 8, 2025  ·  Reported January 28, 2026

Test Category Method Result Status
Vitamins — full panel HPLC Label claims verified ✓ Pass
Thiamine (Vitamin B1) HPLC 7.21 mg/serving (spec: 7 mg) ✓ Pass
Niacin (Vitamin B3) HPLC 31.97 mg/serving (spec: 30 mg) ✓ Pass
Arsenic ICP-MS 0.114 ppm (limit: 15 mcg/day) ✓ Pass
Cadmium ICP-MS 0.065 ppm (limit: 5 mcg/day) ✓ Pass
Lead ICP-MS 0.144 ppm (limit: 5 mcg/day) ✓ Pass
Mercury ICP-MS <LOQ (limit: 15 mcg/day) ✓ Pass
Total Aerobic Plate Count Petrifilm <20 CFU/g (limit: <100,000) ✓ Pass
Coliform Petrifilm <20 CFU/g (limit: <100) ✓ Pass
Yeast Petrifilm <20 CFU/g (limit: <1,000) ✓ Pass
Mold Petrifilm <20 CFU/g (limit: <1,000) ✓ Pass
E. coli qPCR Negative / 10g ✓ Pass
Salmonella qPCR Negative / 10g ✓ Pass
Staphylococcus aureus qPCR Negative / 10g ✓ Pass
Summary: Lot MMV250805 passed all HPLC vitamin label claims, ICP-MS heavy metals screening, and microbiological analysis. All four heavy metals tested well below California Prop 65 and FDA daily intake limits. All microbiological results negative or below detection thresholds.

All products tested in compliance with current Good Manufacturing Practices (cGMP). Testing performed by an accredited independent laboratory. Results are lot-specific and apply to the production run identified above. PeakFusion is committed to publishing updated results when new production lots enter circulation.

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