Product document center
MIT Product Documents & COA Center
Review the product-specific certificates referenced across the Kratom Paradise MIT extract catalog, including sample identifiers, report dates, and direct PDF links.
This center maps current Kratom Paradise MIT extract listings to the laboratory reports they presently reference. The submitted sample identity, analytical result, and finished product must remain distinct in the document chain. Open the current listing and complete PDF together; document relationships can change as products, lots, and records change.
See the 90% label and current sample result together
The current powder line uses the MIT 90% product-line label. Report DD00126B(15) separately lists 87.01% mitragynine for the submitted sample. Read 90% MIT Extract Powder: Product Label vs Current COA Result, then open the standard powder listing or bulk powder listing for current package information.
Current MIT extract document map
| Current listing | Submitted sample | Report date and result | Scope | |
|---|---|---|---|---|
| MIT 90% standard sizes and bulk | DD00126B(15) / SD260715-011 (142956); concentrate matrix | July 20, 2026; 87.01% mitragynine (870.12 mg/g) and 9.08% speciociliatine (90.79 mg/g) | Report describes the submitted concentrate sample; it does not establish every option, size, package, or future lot | Open powder report DD00126B(15) |
| Historical record: retired MIT 60% sample | 141215 / SD260616-036; submitted label MIT 60% | June 23, 2026; 80.43% mitragynine (804.29 mg/g) | Retained for document history only. This sample is not presented as a current product listing or as evidence for the current 90% line. | Open historical report 141215 |
What a referenced report does establish
- The name assigned to the submitted sample.
- The laboratory sample identifier and report date.
- The analytes, units, methods, qualifiers, and results printed on that report.
- The result reported for the material submitted to the laboratory.
What the link does not establish by itself
- That every flavor, size, finished package, or future lot was independently tested under the report.
- That a submitted label value and measured analytical result are identical.
- A serving, equivalency, safety, medical, legal, shelf-life, or resale conclusion.
- That ND means absolute zero; it means not detected at the report's stated threshold.
Read the units before comparing results
| Field | Meaning in the report-reading workflow |
|---|---|
| Percent (%) | A proportion reported for the submitted sample under the laboratory's method |
| mg/g | Milligrams of the reported analyte per gram of the submitted sample |
| ND | Not detected at the laboratory's stated reporting threshold |
| LOD / LOQ | Detection and quantitation limits; use the exact definitions on the report or method |
| Sample ID | The laboratory identifier for the submitted material |
For a full glossary, use How to Read a Kratom Lab Report or COA. For the identity chain, use the batch, lot, and sample ID guide.
Change management
Listings, product options, document links, and reports can be updated. Save the product title, selected option, size, order date, and current report reference with a purchasing or receiving record. Do not rely on a screenshot or old PDF filename without confirming that the live listing still points to the same submitted-sample document.
MIT document FAQ
Why do standard and bulk listings currently link to the same report?
They are related product-line listings that presently reference the same submitted-sample report. That shared reference does not establish independent testing of every package configuration.
Why is the retired MIT 60% report retained?
It is kept as a clearly labeled historical sample record. It does not describe an active product, and it should not be used as the current document for the retail or bulk 90% listings.
Why can the laboratory sample name differ from the retail name?
The retail product is named MIT 90% Mitragynine Extract Powder. The current report identifies submitted sample DD00126B(15) and separately reports 87.01% mitragynine for that sample; the measured result is not the retail product-line name.
Does ND mean the analyte can never be present?
No. ND means the analyte was not detected for the submitted sample at the laboratory's stated reporting threshold.
Document scope: These links map current listings to referenced laboratory files. They do not replace the complete PDF or a product-specific operational record.
Current finished-tablet report
| Current product | Finished-tablet lot | Reported result per unit | |
|---|---|---|---|
| 150mg MIT Mango chewable tablets and bulk tablets | M/150/002; pressed Mitragynine Tablet; issued September 19, 2025 | 146 mg mitragynine, 0.148 mg 7-hydroxymitragynine, and 153 mg total Mitragyna alkaloids per unit | Open tablet report M/150/002 |
The laboratory converted the alkaloid results to mg per unit using a measured tablet weight of 0.921 g. The report does not identify a flavor, so it should not be read as independent flavor verification or as a blanket result for every future lot.
All listed Class I and Class II residual solvents are below the stated limits of quantitation and marked PASS. Acetone is reported at 236 ug/g and marked PASS; the other listed Class III solvents are below the stated limits of quantitation and marked PASS.