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The Tanning Peptide

Melanotan II

Also known as MT-2 · MT2 · The Barbie drug

At a glance

What it is
Tanning and libido peptide with documented case-report harms. We publish no dose.
Evidence
Practitioner experience onlyHow the tiers workThere is no controlled human trial of Melanotan II for tanning or libido. Why this tier
Half-life
Not established in available literature
Routes
Subcutaneous, Intranasal
Category
Sexual health, Skin
FDA
Advisory vote planned
As of 3 August 2026. What that means
WADA
We do not state a status
Amino acids
7

Not schedulable in Claritide. Our sources publish no dosing figure for Melanotan II, so there is nothing to build a schedule from.

Evidence

Why this tier

There is no controlled human trial of Melanotan II for tanning or libido. What exists is a harm literature: multiple case reports of melanoma and rapidly changing pigmented lesions collected by the Skin Cancer Foundation, a case report of eruptive dysplastic naevi, and one verified emergency-medicine case report of rhabdomyolysis and sympathomimetic toxicity after a 6 mg subcutaneous dose. Note what Cancer Research UK does not say: it makes no specific melanoma-causation claim, which tells you the melanoma link is case-report-tier rather than established.

Overview

What it is

Melanotan II is a non-selective melanocortin agonist sold for tanning and libido. It is not approved for any use anywhere we could verify, it is illegal to sell and supply in the UK, and its harm literature includes a verified emergency-medicine case report of severe systemic toxicity. We deliberately publish no dose range for it. The only dose figure we can state is the one that put someone in intensive care.

Mechanism

How it works

Melanotan II is a synthetic analogue of alpha-melanocyte-stimulating hormone that activates melanocortin receptors without much selectivity between them. MC1R activation on melanocytes drives eumelanin production, which is the tanning effect. MC4R and MC3R activation in the central nervous system is the route to the appetite and sexual-arousal effects. Because it hits several receptors at once, the effects it is bought for and the effects it is not arrive together: pigment changes, nausea, flushing, and, through sympathomimetic activity, cardiovascular effects. There is no way to select for one arm of that.

Dosing

Commonly researched ranges

These are figures reported in published literature and practitioner protocols: a commonly researched range, not a recommendation. Claritide does not tell you what to take.

Not established in available literature. Our sources describe Melanotan II without publishing a dosing figure, so Claritide does not print one.

Cycle guidance
Not established in available literature
Goals
Libido, Skin & hair
Legal standing

Where this sits with the FDA

Dated, sourced, and separate from whether it works. Removal from a warning list is not permission to compound.
Advisory vote plannedas of 3 August 2026 · US

FDA 503A bulks · nomination withdrawn; FDA says it will hold an advisory committee meeting on it before the end of February 2027

Removal from Category 2 is not permission, and the picture outside the US is unambiguous: Melanotan nasal sprays and injections are illegal to sell and supply in the UK, Australian regulators have warned against melanotan tanning products sold illegally online, and Melanotan I and II sit on FDA Import Alert 66-41. The Skin Cancer Foundation stated on 7 July 2026 that Melanotan II is not FDA-approved for any use and its safety has not been established.

Last change · 22 April 2026 · Melanotan II was among the 12 peptides removed from Category 2, effective 22 April 2026, and FDA says it will hold an advisory committee meeting on it before the end of February 2027.

Primary source

How it got here

  1. 18 September 2019

    Melanotan I and II added to FDA Import Alert 66-41: "The product is imported as non-human research purposes only and then the unapproved new drug is sold on internet."

  2. 15 April 2026

    FDA announced a future Pharmacy Compounding Advisory Committee meeting to discuss Melanotan II, alongside GHK-Cu, Cathelicidin LL-37, dihexa acetate and PEG-MGF, with its time and place still to be scheduled.

  3. 22 April 2026

    Removed from Category 2 in the April 2026 tranche. Some vendor pages report this as contested; it is not, and removal is not permission.

  4. 7 July 2026

    The Skin Cancer Foundation issued a press warning: not FDA-approved for any use, safety not established, with case reports of melanoma and rapid changes in moles following use.

  5. 28 February 2027

    FDA says its Pharmacy Compounding Advisory Committee will meet before the end of February 2027, on a date not yet set.

An advisory vote is not law. In July 2026 an FDA advisory committee voted in favour of adding several peptides to the 503A bulks list, over the explicit recommendation of FDA’s own scientific reviewers, who recommended against all seven. FDA would still have to write a rule, and it has not proposed one or given a date. None of these compounds is lawfully compoundable today.Note what FDA actually assessed: BPC-157 for ulcerative colitis, TB-500 for wound healing, KPV for wound healing and inflammatory conditions, MOTS-c for obesity and osteoporosis, Epitalon for insomnia, Semax for cerebral ischaemia, migraine and trigeminal neuralgia. Whatever emerges from rulemaking will be scoped to those indications.

Sport

WADA status

The 2026 Prohibited List entered force on 1 January 2026.
We do not state a status

Not named on the 2026 Prohibited List. We could not determine whether the S0 catch-all applies and do not state a status.

We looked and could not resolve it. This is not the same as "not prohibited". Treat it as unresolved and check with your federation before competing.

The FDA reclassification has no effect whatsoever on WADA status.

Reconstitution

Mixing recipes our sources document

Concentration (mg/mL) = vial mg ÷ diluent mL. On a U-100 barrel, 1 unit = 0.01 mL.

Not established in available literature. Use the calculator with the figures printed on your own vial.
Open the calculator

Expectations

Week by week

What our material describes people reporting. Individual responses vary widely.

Not established in available literature.

Tolerability

Side effects

Grouped by how often our sources report them. Percentages appear only where a published trial figure exists.

Common

  • New and rapidly changing moles and pigmented lesionsThe Skin Cancer Foundation, in a press statement dated 7 July 2026: "Case reports have documented the development of melanoma following Melanotan II use, as well as rapid changes in moles and pigmented lesions." Atypical naevi are established melanoma precursors. Causation for melanoma itself is not established: this is case-series-level evidence, and both halves of that sentence matter.
  • Nausea and flushingConsistent with non-selective melanocortin agonism, and the same profile documented on the approved bremelanotide label.

Uncommon

  • Eruptive dysplastic (atypical) naeviCase report in Actas Dermo-Sifiliográficas, including a teenager with familial atypical multiple mole melanoma syndrome.

Rare

  • Rhabdomyolysis with sympathomimetic toxicity and renal dysfunctionVerified primary case report: Nelson, Bryant and Aks, Clinical Toxicology 2012, PMID 23121206. A 39-year-old man self-injected 6 mg subcutaneously. Blood pressure 151/85, heart rate up to 146, dilated pupils, tremor. Creatine kinase rose from 1,760 to 17,773 IU/L with myoglobinuria and red cell casts. Three days in intensive care on fluids and bicarbonate.
Safety

Contraindications and interactions

Do not use if

  • Any personal or family history of melanoma, atypical naevi or dysplastic naevus syndrome: the case-report literature is concentrated here
  • Any new, changing or asymmetric mole. Stop and see a dermatologist rather than reading a peptide page
  • Melanotan nasal sprays and injections are illegal to sell and supply in the UK, and Australian regulators have issued warnings about the same products

Interactions

Not established in available literature.

Absence from this list does NOT mean safety. It means lack of research.

Handling

Storage and cost

Storage
We publish no handling protocol for Melanotan II. Doing so would imply a use we are declining to normalise, and the products in circulation are, in Cancer Research UK’s words, untested for safety, quality or effectiveness and may contain harmful chemicals not listed on the label.
Cost
Not established in available literature
Deep dive

Melanotan II in full

A deliberate decision

This record publishes no dose range. Not because we could not find numbers, since every vendor blog has them, but because every source with numbers is a vendor blog, and printing them would normalise a protocol we have no basis to normalise.

The one dose figure we can state is the toxic one, and it is on this page.

What it is

Melanotan II is a synthetic analogue of alpha-melanocyte-stimulating hormone that activates melanocortin receptors without much selectivity. MC1R activation on melanocytes drives eumelanin production, the tan. MC4R and MC3R activation in the central nervous system produces the appetite suppression and sexual arousal it is also bought for.

Because it hits several receptors at once, you do not get to pick. Pigment changes, nausea, flushing and sympathomimetic cardiovascular effects arrive with everything else.

Note the naming: "the Barbie drug" is Melanotan II. The nickname migrates onto PT-141 in community writing, and it carries the wrong expectations when it does.

The verified toxicity case

Nelson, Bryant and Aks, Clinical Toxicology, 2012, PMID 23121206. A 39-year-old man self-injected 6 mg subcutaneously. He presented with blood pressure 151/85, heart rate rising to 146, dilated pupils and tremor. Creatine kinase went from 1,760 to 17,773 IU/L, which is rhabdomyolysis, with myoglobinuria and red cell casts in the urine. He spent three days in intensive care on fluids and bicarbonate.

That is a verified, primary, emergency-medicine case report of a single self-administered dose putting someone in intensive care.

The pigmentation and melanoma picture, stated honestly

Both halves, because either one alone misleads.

The Skin Cancer Foundation, in a press statement dated 7 July 2026, states verbatim: "Case reports have documented the development of melanoma following Melanotan II use, as well as rapid changes in moles and pigmented lesions." A separate case report in Actas Dermo-Sifiliográficas describes eruptive dysplastic naevi following melanotan use, including in a teenager with familial atypical multiple mole melanoma syndrome.

Melanotan II stimulates melanocytes. It is associated in case reports with new and changing atypical moles, which are established melanoma precursors.

And causation for melanoma itself is not established. The evidence is case-series level. Cancer Research UK, which reviews this territory carefully, makes no specific melanoma-causation claim: it says the products are not safe to use, have not been tested for safety, quality or effectiveness, and could contain harmful chemicals not listed on the label. What a careful organisation declines to say is informative.

Three further harms circulate widely and we do not state them, because we could not retrieve the papers: an oral mucosal melanoma after nasal-spray use, ischaemic priapism requiring surgical decompression, and posterior reversible encephalopathy syndrome with renal infarction. Unverified means unverified.

Regulatory position

Not approved for any use. Illegal to sell and supply in the UK. Australian regulators warn against melanotan tanning products sold illegally online, including nasal sprays and injectables. Melanotan I and II have been on FDA Import Alert 66-41 since 18 September 2019, with the entry noting the pattern precisely: imported for stated non-human research purposes, then sold on the internet as an unapproved new drug.

In the US it came off Category 2 in April 2026, and FDA says it will hold an advisory committee meeting on it before the end of February 2027. Some vendor pages present the US position as contested. It is not, and removal from Category 2 has never meant permission.

The nasal sprays

The nasal spray is the current enforcement problem in the UK and Australia, and it is worth understanding why it spreads: no needle, no visible administration, and a mental model that a spray must be gentler than an injection. Nothing about the receptor pharmacology changes with the delivery device.

References

Sources

  1. 1
    The Skin Cancer Foundation, 7 July 2026 · warning regarding Melanotan II
  2. 2
    Cancer Research UK · Fake tan and melanotan injections, last reviewed 30 November 2023
  3. 3
    Nelson, Bryant, Aks, 2012 · rhabdomyolysis and sympathomimetic toxicity after 6 mg subcutaneous Melanotan II, Clin Toxicol (Phila)
  4. 4
    Actas Dermo-Sifiliográficas · Eruptive dysplastic naevi following melanotan use
  5. 5
    FDA · Meeting of the Pharmacy Compounding Advisory Committee, to be held before the end of February 2027, on cathelicidin LL-37, GHK-Cu, dihexa acetate, Melanotan II and PEG-MGF (content current as of 15 April 2026)
  6. 6
    FDA Import Alert 66-41 · Melanotan I and II listed 18 September 2019

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