This production lot was tested for ingredient potency, identification, capsule weight, disintegration, heavy metals, and microbial quality.
| Test |
Claim or Limit |
Result |
| Potency |
| Pregnenolone |
95-110 mg |
96 mg |
| Identity Testing |
| Identification |
Conformity (sample retention time corresponds to standard) |
Conforms |
| Physical Testing |
| Capsule Weight |
238-277 mg |
257.5 mg |
| Disintegration |
Not more than 30 minutes |
Not more than 30 minutes |
| Heavy Metals |
| Arsenic |
<1.5 ppm |
<0.000 ppm |
| Cadmium |
<0.5 ppm |
0.000 ppm |
| Lead |
<1.0 ppm |
0.052 ppm |
| Mercury |
<0.2 ppm |
<0.000 ppm |
| Microbial Testing |
| Total Plate Count |
<1,000 CFU/g |
<1,000 CFU/g |
| Total Yeast & Mold Count |
<100 CFU/g |
<100 CFU/g |
| E. coli |
<0.1 CFU/g |
<0.1 CFU/g |
| Salmonella spp. |
<0.1 CFU/g |
<0.1 CFU/g |
| Staphylococcus aureus |
<0.1 CFU/g |
<0.1 CFU/g |
View Certificate of Analysis (PDF)
See the original Certificate of Analysis for complete testing details, methods, and laboratory documentation.