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PEPTIDE ATLAS / SKIN & HAIR / MELANOTAN II

Not FDA-approvedInsufficient

Melanotan II

Editorial visualization for skin & hair peptide research
THE SIGNAL MAP · SKIN & HAIR
ALSO KNOWN ASMT-2 · tanning peptide

An unapproved tanning peptide linked to serious case reports and unpredictable products.

01CATEGORYSkin & hair
02REGULATORY STATUSNot FDA-approved
03COMMON ROUTETypically sold for subcutaneous injection or nasal use; neither is approved
04DOSE BASISHuman study + reported community use

HOW TO USE THIS PAGE

Read the profile in the order that protects the decision.

  1. 01
    Verify what it is

    Confirm the exact molecule, route, regulatory lane and actual human evidence.

  2. 02
    Read limits before dose

    Unsupported claims, contraindications and uncertainty come before any protocol.

  3. 03
    Build the monitoring plan

    Define the target, baseline checks, reassessment point and stop rules with a qualified clinician.

IMPORTANT STATUS CHECK

This peptide does not have an FDA-approved product or dose for the claims described here. Research dosing and vendor protocols are not consumer prescribing guidance.

RESEARCH PASSPORT

The five facts to know first.

REVIEWED
JULY 2026

HUMAN EVIDENCEInsufficient

Evidence strength for the context described on this page.

REGULATORY LANENot FDA-approved

Status is product-, formulation- and indication-specific.

DOSE FOUNDATIONHuman study + reported community use

Trial, label or reported-practice basis is always named.

SOURCE PACK5 original references

Official labels, regulators, trials and indexed literature where available.

TESTED ATHLETESVerify the exact ingredient.

Peptide hormones, growth factors and related substances may be prohibited.

Check Global DRO ↗

OVERVIEW

What Melanotan II is.

A synthetic melanocortin analog sold for tanning and sometimes sexual effects. It is not afamelanotide and has no FDA-approved consumer use.

HOW IT IS THOUGHT TO WORK

Nonselectively activates melanocortin receptors, influencing pigmentation, appetite, cardiovascular responses and sexual function.

EFFECTS & EVIDENCE

What the evidence supports—and what it does not.

SUPPORTED IN CONTEXT
  • Can darken skin
  • Pigmentation is not evidence of safe photoprotection
NOT ESTABLISHED
  • Safe tanning
  • Skin-cancer prevention
  • Safe erectile or libido enhancement
  • A standardized human dose

Evidence grade: Insufficient. For an approved drug, “high” refers only to its labeled indication—not every off-label or wellness claim.

DOSAGE CONTEXT

Best available dosing range.

Human study + reported community useBest human-research range: 0.01–0.025 mg/kg subcutaneously in a small phase 1 program; severe nausea occurred at 0.025 mg/kg in some subjects. Current users and clinics more often publish 0.25–0.5 mg daily for loading, followed by 0.25–0.5 mg once or twice weekly. The market range is not approved and should not be interpreted as a safe consumer standard.
BEST AVAILABLE GENERIC RANGE

Men and women.

The basis is named above. Reported-use ranges describe what clinics or communities publish; they are not proof of safety, efficacy, legality or product quality.

MENReported tanning-use range: 0.25–0.5 mg subcutaneously daily during a 7–14 day loading period, then 0.25–0.5 mg once or twice weekly. Priapism is a male-specific emergency risk.
WOMENReported tanning-use range: 0.25–0.5 mg subcutaneously daily during a 7–14 day loading period, then 0.25–0.5 mg once or twice weekly. Pregnancy safety is unknown.
Schedule in that source context
Commonly reported as daily loading for 1–2 weeks, then once- or twice-weekly maintenance. Long-term safety has not been established.
How to interpret it
The early study dose of 0.025 mg/kg is not a consumer recommendation and produced frequent nausea. Current market ranges are unapproved and product identity is unreliable. UV exposure adds independent skin-cancer risk.
ACTUAL HUMAN DOSES REPORTED IN THE RECORD

Research regimens may use different routes, diagnoses, formulations and monitoring. They cannot automatically be converted into a general protocol.

  • Early phase 1 tanning research: 0.01–0.025 mg/kg subcutaneously for five doses given every other day; investigators selected 0.025 mg/kg for future study.
  • Erectile-response studies in men also used 0.025 mg/kg subcutaneously; severe nausea occurred in a subset.
Route
Typically sold for subcutaneous injection or nasal use; neither is approved
Duration
Reported loading: 7–14 days; maintenance may continue, but no safe long-term course exists
Men & women
The reported tanning range is similar for men and women, but male priapism risk and unknown pregnancy/reproductive safety require separate counseling.

Clinician verification required. Always double-check the exact molecule or salt, concentration, route, volume, schedule, indication, patient-specific contraindications, interactions and applicable law with the prescribing clinician and dispensing pharmacy. A disclaimer does not make an unapproved product FDA-approved, and a reported-use range is not a prescription.

MONITORING

What should be tracked.

  • New or changing pigmented lesions require dermatology evaluation
  • Blood pressure and prolonged erection are acute concerns

SAFETY

Risks, red flags and reasons to avoid it.

KNOWN OR PLAUSIBLE RISKS
  • Nausea, flushing, blood-pressure effects and spontaneous erections
  • Priapism
  • FDA cites case reports including melanoma, posterior reversible encephalopathy syndrome and sympathomimetic toxidrome
  • Contamination and incorrect identity
AVOID / ESCALATE
  • Human use
  • History of concerning pigmented lesions
  • Cardiovascular disease
  • Combining with sexual-function drugs
Stop and seek careGet urgent medical help for trouble breathing, facial or throat swelling, chest pain, fainting, severe persistent abdominal pain, neurologic changes, severe hypoglycemia, uncontrolled vomiting or a prolonged painful erection.

CLINICIAN VISIT CHECKLIST

Six questions worth bringing with you.

01What exact product is this?

Molecule or analog, salt, concentration, route, manufacturer or compounder, lot and beyond-use date.

02What outcome are we treating?

Name the diagnosis or target, how it will be measured and the realistic time to reassess.

03Why this option?

Ask how it compares with FDA-approved, lower-risk or better-studied alternatives.

04Where did the dose come from?

Label, human trial, specialty guideline or clinic convention—and whether that route and formulation match.

05What is the monitoring plan?

Baseline checks, follow-up measures, interactions, pregnancy considerations and symptoms that mean stop.

06How is quality verified?

Pharmacy license, prescription, identity/potency testing, sterility controls and who handles a product complaint.

Do not improvise reconstitution or convert “units” without the exact concentration. Mixing, storage and beyond-use instructions are product-specific; confirm them with the dispensing pharmacy.

PRIMARY SOURCES

Read the record yourself.

We prioritize official prescribing information, FDA regulatory material, registered trials and indexed biomedical literature. A source supports the specific statement beside it—not every claim made about the molecule.

PRODUCTS & TREATMENT ACCESS

There is no product we can responsibly recommend.

AVAILABILITY

Illicit/gray-market online product; not FDA-approved.

MARKET REALITY

A tan is a visible pharmacologic effect, which can make an unsafe product feel effective. It does not establish product quality or long-term safety.

NO COMMERCE RECOMMENDATION

Evidence before affiliate revenue.

We do not rank or sell unapproved research peptides. Use the Atlas to discuss safer, evidence-backed alternatives with a qualified clinician.

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