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Proviron Mesterolone - Xeno Laboratories

Xeno Laboratories

Proviron Mesterolone - Xeno Laboratories

Oral · 25 mg/tab · 50 tabs

Out of stock
CompoundMesterolone
ClassOral androgen
Half-life12-13 hours
Detection10-14 days urine
Liver toxicityLow
Water retentionNone
A 25 mg tablet of a DHT-derived oral androgen that is not 17-alpha-alkylated, which is why its hepatic reputation is milder than that of most oral steroids. It does not convert to estrogen, so it adds no fluid or breast risk, and it binds the protein that carries testosterone, which can free up a little more of the active hormone. It is a supporting androgen, not a mass or cutting drug, and it does not restore the axis.
Proviron Mesterolone - Xeno Laboratories
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All products are manufactured under strict quality standards and independently tested before release. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Product Overview

Xeno Laboratories Proviron is mesterolone at 25 mg per tablet, an orally active androgen derived from dihydrotestosterone with a strong androgenic character and only a weak anabolic one. It is a support product in the truest sense of the term on this line: it is taken beside a course to add androgen tone and to nudge the free fraction of testosterone upwards, and it is never the reason a user gains size or gets leaner.

Two chemical facts explain its behaviour. The first is that it does not aromatise, so nothing in it converts to estrogen and it cannot produce the fluid retention or the breast sensitivity that a converting compound can. The second is that it is one of the few oral androgens that is not 17-alpha-alkylated, which is why its hepatic profile is described as milder than that of most oral steroids even though it is swallowed rather than injected. The half-life is 12 to 13 hours, so the daily amount is normally divided, and the metabolite picture is what makes it detectable in urine for ten to fourteen days and often longer.

Its best-documented action at the protein level is on sex hormone binding globulin. By occupying that carrier, mesterolone can raise the free, unbound share of circulating testosterone without adding any testosterone itself, which is why it turns up beside a testosterone course rather than on its own. Users who are managing hair loss with Finasteride or Avodart have to weigh that against the fact that mesterolone is itself a DHT-derived androgen.

Dosage Protocol

Amounts below are reference steps for the substance rather than a prescription, and they assume a divided daily intake. Nothing above 100 mg a day is supported by the sources.

Beginner 25 mg a day, split when convenient, for the length of the supported course
Intermediate 50 mg a day, usually taken in two portions
Advanced 50-100 mg a day; the higher figure is the top of the documented range
Female Not recommended, because the androgenic effects are strong and virilization is a real risk
Administration Oral, divided across the day because the half-life is only about half a day
Duration Matched to the course beside it, with no independent cycle of its own

The clinical reference point differs from the sports one, which is worth knowing because it explains the tablet size. In replacement therapy the substance is given at 25 mg two or three times a day, so the 25 mg unit is a medical step. Sports use usually settles lower than that, and the higher rows exist for want of a better description rather than because they are needed.

Suggested Protocols

Where the tablet sits in a plan is narrow, and it is always a supporting position. The three arrangements below reflect how the sources describe its use.

Androgen side of a converting course
Taken for the length of the course; the androgen tone and the estradiol reading are the two things being watched
Androgen tone on a dry course
A low amount beside an injectable, chosen because the tablet adds no fluid of its own
Where the plan goes afterwards
Proviron - withdrawn with the course + Tamox - the recovery stage + Clomiphene - the other SERM route
The tablet is not part of recovery; it stops when the course does and the SERM takes over from there

What to Expect

  • Androgen tone, meaning libido and a denser look, usually becomes noticeable in the first week or two.
  • Free testosterone can rise because the tablet ties up the protein that normally carries it, without any extra testosterone being added.
  • Fluid retention and breast risk do not appear from the tablet, because it does not convert to estrogen.
  • Androgenic effects can show up instead: acne, hair shedding and, in prolonged use, voice change.
  • It does not deliver meaningful anabolic effect, and the sources describe its anabolic power as weak.
  • It does not replace a testosterone base, and it does not restore a suppressed axis at the end of a course.

Side Effects and Management

VirilizationAcne, hair loss and voice changes are dose-dependent; lower the amount and reassess.
Raised libidoExpected from an androgen; manage with the dose rather than with another product.
Lower HDL and lipid shiftsKeep a lipid panel on the schedule, particularly with oral androgens stacked.
Mild axis suppressionPlan the recovery step around the whole course, not around this tablet alone.
Stomach irritationTake it with food and divide the daily amount if the stomach reacts.
Hair-loss conflictA DHT-derived androgen works against a 5-alpha reductase inhibitor; decide which goal matters more.

Cycle Support and Follow-Up

This tablet is not a recovery product. Its own suppression of the axis is mild, but the course it accompanies is the thing that has to be reversed, so the post-cycle plan belongs to that course and not to this page.

OnsetNot applicable: the tablet does not open or close a recovery window of its own
Option ATamox 40 mg for the opening week and 20 mg afterwards, aimed at the main course
Option BClomid 50 mg a day for four weeks, the second route to the same recovery
Low-dose cyclesA light course may need a SERM alone, with no gonadotropin block in front of it
Dose ceilingDocumented use stops at 100 mg a day; higher amounts are not supported by the sources
Follow-upTotal testosterone, luteinising and follicle stimulating hormone, estradiol and a lipid panel

The androgen question does not end here, and the pages that pick it up are Finasteride and Avodart for the DHT side, Aromasin for the alternative estrogen tool, and HCG 5000 IU for the injected step that often precedes recovery.

This page is published for educational and research reference only. The compound described is a research-grade material supplied for laboratory work and is not presented here as a medicine or as a treatment for any condition. Dosing information reflects published clinical and reference data for the active substance, not a recommendation or a prescription. Hormonal decisions belong with blood work and a clinician, and nothing here should be read as medical advice. Keep all products out of reach of children and follow the regulations that apply in your country.
What is Xeno Proviron (mesterolone)?
Mesterolone, 25 mg to a tablet, an oral androgen derived from DHT with strong androgenic and weak anabolic activity. It is taken beside a course rather than on its own, it does not convert to estrogen, and it is one of the few oral androgens that is not 17-alpha-alkylated.
How does mesterolone work on a cycle?
Its main documented action is on sex hormone binding globulin. By occupying that carrier protein it can raise the free share of circulating testosterone, and it adds androgen tone from its own androgenic character. It is not a mass builder, and the sources describe its anabolic power as weak, so it supports a plan rather than driving one.
Proviron dosage per day?
Reference sports amounts run from 25 mg a day to 50 mg a day, with 50-100 mg daily as the top of the documented range and nothing above it supported. Because the half-life is 12 to 13 hours, the daily total is normally split. The medical replacement schedule is higher, at 25 mg two or three times a day, which is not the same setting.
Does it raise testosterone?
Not in the sense of adding any. What it can do is displace testosterone from the protein that carries it, so the free, biologically available fraction goes up while the total stays close to where it was. That is a different claim from raising production, and it is the one the sources actually support.
Does it cause gynecomastia or water retention?
Neither belongs to this tablet, because it does not aromatise and so produces no estrogen to act on breast tissue or to hold fluid. Where those problems appear on a plan, they come from a converting compound, and the tools for them are Arimidex or, for an established receptor problem, a SERM such as Tamox.
Can it be stacked with finasteride or dutasteride?
The two goals pull against each other. A 5-alpha reductase inhibitor such as Finasteride or Avodart exists to reduce DHT, while mesterolone is itself a DHT-derived androgen. Running both is possible but the user should decide which outcome matters more and keep the amounts low.
Is Proviron a recovery drug?
No. It is an androgen, and androgens do not restart the axis; if anything they add to the suppression. Recovery after a course is the job of a SERM such as Clomiphene, and the tablet stops when the course stops.
What are its main side effects?
Androgenic effects head the list: acne, hair shedding, a rise in libido and, with extended use, deepening of the voice. Shifts in the lipid picture and mild suppression of the axis are also reported. They are dose-dependent, which is why the reference range stops at 100 mg a day and why most plans use far less.

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