Serrapeptase Comparison Guide

Comparing Serrapeptase? Look Beyond the Front-Label SPU.

When products lead with different SPU numbers, use the same four questions for each one: What activity is declared per capsule? How is delayed release built? What was tested on the finished dosage form? Can the evidence be traced to the bottle lot?

Activity · Delivery · Finished-Product Testing · Traceability

Same questions. Same standard. Then compare the evidence.

iSerra Serrapeptase 250,000 SPU bottle
ActivitySPU per capsule
DeliveryDefined delayed-release architecture
Finished-product testingNamed finished-product method
TraceabilityBottle lot → evidence record
Use the Same Standard

Four criteria make serrapeptase claims easier to compare.

The goal is not to chase the largest number. It is to understand what the number means, how the dosage form is built, what was tested on the finished product, and how much evidence is actually inspectable.

1

Activity

Is enzyme activity stated in SPU per capsule, with serving size and ingredient weight clearly separated?

2

Delivery

Does the product explain its delayed-release architecture, rather than relying on a vague protection statement?

3

Finished Product

Is there testing on the finished dosage form that documents gastric resistance and intestinal-phase disintegration?

4

Traceability

Can the bottle lot be connected to results, methods, test dates, and available source documentation?

Separate Architecture from Testing

What is built and what is measured are different questions.

A delivery-system name should describe the dosage-form design. A finished-product test should document how the completed dosage form behaved under the stated method. Those are related, but they are not interchangeable.

Bilamex™ describes the delivery architecture.

Bilamex™ is iSerra's two-stage physical delayed-release design. It describes how the dosage form is built, not a test result or a promised health outcome.

  • Stage 1: delayed-release capsule.
  • Stage 2: coated enzyme-containing particles.
  • Architecture is disclosed separately from finished-product testing.

USP <2040> documents finished-product behavior.

Finished-dosage-form disintegration testing is reported separately so a buyer can distinguish the formulation architecture from measured gastric-resistance and intestinal-phase disintegration performance.

  • Finished-product method is identified.
  • Lot-specific status is reported when available.
  • The result is a dosage-form test, not a clinical efficacy study.
Now Apply the Framework to iSerra

Here is what iSerra discloses for each criterion.

Apply the same four criteria to any serrapeptase label. The right column shows the disclosures iSerra provides for each category.

CriterionWhat to inspectiSerra disclosure
ActivitySPU per capsule, serving size, ingredient weight, and whether a lot-specific measured activity result is available.250,000 SPU declared per capsule; current shipping lot 6798 reports 292,327 SPU measured activity.
DeliveryThe physical dosage-form architecture used to delay release through the gastric phase.Bilamex™ Dual-Phase Delivery: delayed-release capsule + coated enzyme-containing particles.
Finished-product testingTesting performed on the finished dosage form, with the method identified.USP <2040> disintegration testing is identified; current lot status: Pass — USP <2040>.
TraceabilityA lot-specific record tied to the bottle, including methods, dates, results, and supporting records when available.Veriphase™ Lot Verification connects a production lot to the available verification record and supporting source documentation when available.
Lot-Specific Evidence

See what lot-specific evidence looks like in practice.

Production lots change. The lot printed on the bottle is the authoritative lookup key. The current shipping lot is shown for context, and a specific bottle can be checked by its own lot number.

VERIFY A LOT NUMBER
Production Lot 6798Tested 2026-08-05
Measured Activity292,327 SPU
Declared Specification≥ 250,000 SPU/capsule
IdentityConfirmed
Heavy MetalsPass
Microbial LimitsPass
DisintegrationPass — USP <2040>
LaboratoryIndependent ISO 17025-accredited laboratory
Activity MethodUSP proteolytic assay
Only fields actually recorded for this lot are shown. Supporting laboratory documentation is provided when available. Product testing documents specifications and dosage-form performance; it does not establish a clinical outcome.
Comparison Questions

Know what the evidence can—and cannot—tell you.

Is a higher milligram amount the same as higher serrapeptase activity?

No. Milligrams describe ingredient weight; SPU describes enzyme activity. Compare the stated activity units and serving size rather than using weight alone as a proxy for potency.

Does a measured lot result replace the 250,000 SPU label claim?

No. 250,000 SPU per capsule is the declared specification. A measured activity result belongs to a specific production lot and can vary from one lot to another.

What is Bilamex™ Dual-Phase Delivery?

Bilamex™ describes the physical dosage-form architecture: a delayed-release capsule surrounding coated enzyme-containing particles. It is separate from finished-product disintegration testing.

What does USP <2040> testing show?

It is finished-product disintegration testing used here to document the dosage form's gastric resistance and intestinal-phase disintegration behavior. It does not establish a clinical outcome.

Can I verify the lot on my own bottle?

Yes. Enter the production lot printed on your bottle on the Verify Your Lot page to access the applicable available record.

This guide compares disclosed product attributes and testing categories, not medical outcomes or competing brands.

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Consult your healthcare professional before use, especially if pregnant, nursing, taking blood thinners, or scheduled for surgery.
Next Step

Evidence first. Pricing and purchase options second.

If these four comparison criteria match what you want to inspect, continue to the dedicated iSerra purchase page for current pricing, one-time and subscription choices, supply options, guarantee terms, and checkout.

VIEW ISERRA PRICING & PURCHASE OPTIONS
iSerra®

Evidence & Comparison Guide for evaluating disclosed serrapeptase product attributes.

Verify your iSerra lot

Enter the lot number printed on your bottle. The verification stays on this page.

Use the production lot exactly as printed on the bottle label.