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Melanotan I (Afamelanotide)_Dosage, benefits & legal status

Also known as afamelanotide, Scenesse, MT-1, Melanotan I

Published July 22, 2026 · Updated August 14, 2026

A tanning peptide. The FDA-approved version is an implant for a rare sun-pain condition.

Tanning & skin protectionMelanocortin agonistResearch only
Common vial size10 mg
Dose0.5 up to 1 mg per day (loading phase)
FrequencyDaily then weekly
RouteUnder the skin (or implant)
StatusResearch only (approved implant exists)
CycledThe approved implant is one every 2 months, about 3 a year

Common vial size is what vendors typically sell, not a recommendation. Enter your own vial in the calculator.

01

What is Melanotan I (Afamelanotide)?

Plain language first. The technical label stays, but it never stands alone.

Overview

It builds a slow, even, protective tan and shifts your skin toward real sun defense. It is FDA-approved (as Scenesse) for a rare light-sensitivity disorder.

The technical version

Melanotan I (afamelanotide) is an analog of alpha-MSH, the hormone that tells skin to make the pigment melanin.

What it's used for

The safer, approved tanning peptide. It builds a slow, even, protective tan and shifts skin toward real sun defense. It has fewer side effects than its cousin, but is slower and pricier.

02

How does Melanotan I (Afamelanotide) work?

What it does in the body, and where.

Melanotan I copies alpha-MSH, the hormone that tells skin to make pigment. It is the only compound in this pair that is an approved medicine.

  1. 01
    It activates the MC1R receptor in skin
    The pigment switch, prompting melanocytes to produce eumelanin.
  2. 02
    The tan is protective, not cosmetic in intent
    Eumelanin genuinely absorbs UV, which is the basis of its approved use.
  3. 03
    It is selective for MC1R
    Which is what separates it from Melanotan II and why it lacks the libido and appetite effects.
  4. 04
    Approved for a rare condition
    As Scenesse, for erythropoietic protoporphyria, where sunlight causes severe pain. Given as an implant, not an injection.
Where it acts
Skin

Where this compound is thought to act.

03

What else is it used for?

Each use below carries its own evidence level. Approved means regulators have cleared it for that purpose. Investigational means it is in trials. Early research means it is being studied and is not established.

  • Preventing pain and skin damage in a rare light-sensitivity disorder, sold as Scenesse. This is its approved useFDA-approved
  • Building a slow, even tan, which is why most people who buy it want it. This use is not approved and the product sold online is not ScenesseResearch only
  • Shifting skin toward genuine sun protection rather than just colorEarly research

The published record

Research index

146

Records indexed for Melanotan I (Afamelanotide)

103 in humans, 48 of them original studies.

23 registered trials, 12 with posted results.

FDA: Named on the alert (Melanotan I and II).

Browse the records

In animalsPro
In the labPro
ReviewsPro
Senior author sharePro

Counted from Europe PMC indexing, not read by a person. Human means indexed under humans, which includes reviews and work on human cells. Original studies exclude reviews and lab work on human cells.Last updated 11 September 2026.

Melanotan I (Afamelanotide) vial rendering
Compound field notes

At a glance

Four things to know about Melanotan I (Afamelanotide)

01

Evidence

Research only

02

Category

Skin and cosmetic

03

Common vial

10 mg

04

Half-life

About 15 hours as the implant, about 30 minutes injected

04

How much, and do you cycle it?

The range, and whether you take breaks.

0.5 up to 1 mg per day (loading phase), daily then weekly. The approved implant is one every 2 months, about 3 a yearFDA label

The approved product is an implant placed every two months, typically three times a year to cover spring and summer. That interval is on the label. The injectable version sold separately is a different product used on a loading-then-maintenance pattern that comes from community practice.

Source: SCENESSE (afamelanotide) FDA label

Compare this against the whole library →

05

How long does it stay in the body?

The half-life, and where the figure comes from.

About 15 hours as the implant, about 30 minutes injectedFDA label

Two very different numbers for the same molecule. The approved product is a controlled-release implant and its 15 hours reflects how slowly the implant releases, not how fast the peptide clears. Plain injected afamelanotide clears in about 30 to 33 minutes.

Source: Scenesse label, DailyMed setid 94f53286-11dd-7fbb-e053-2a95a90a7c48

You can compare this against the whole library to see where it sits.

06

How do I dose and price it?

Enter your vial and your dose. Pick a mix. We show the draw and the cost.

The vial holds a fixed amount of drug. Adding more water does not make more drug, it just spreads it thinner, so you draw a bigger number on the syringe for the same dose.

Your vial size (mg)
Printed on the vial.
What you paid per vial
$
Used for cost per dose only.
Your dose (mg)
Commonly referenced range: 0.5 up to 1 mg per day (loading phase)Community practice

Choose your mix

your own mL
units · —
Enter your own volume

Measuring the water1 mL = one full 100-unit syringe.

Your draw

10 / 100 units
What it costs

Melanotan I (Afamelanotide) starts at $21.05 across 31 vendors, typically $2.60 – $5.90 per mg.

38 listings, last read Sep 5, 2026. Shipping and card fees are not included.

See all 38 listings →
07

How do you store it?

Before mixing, and after.

Dry powder in the freezer or fridge. Once mixed, fridge, and use within about a month.

Unmixed lyophilized Melanotan I (Afamelanotide) keeps for a long time cold. Once you add water the clock starts: most reconstituted vials hold up for roughly 28 to 30 days at fridge temperature. Keep it out of light, and do not freeze it after mixing.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.

Who should avoid it

Check these before anything else.
  • Pregnancy
  • Approved only for a specific rare light-sensitivity disorder

Stop and get help

These are emergencies. Seek care.
  • A mole that changes in size, shape, or color
  • Signs of an allergic reaction

Common effects

Expected, and usually mild.
  • Darkening of skin, which is the intended effect
  • Nausea
  • Headache
  • Reactions at the implant site

Where this page says nothing is established, that means nobody has studied it, not that a compound is safe.

09

Is Melanotan I (Afamelanotide) approved?

And where the numbers on this page come from.

No. Melanotan I (Afamelanotide) is not approved for any use, anywhere. It is sold labelled for laboratory research only, and there is no legal route to buy it for human use.

  • Injected under the skin
    Research onlyNot approvedThe reconstituted vial sold for tanning is not the approved product and is not approved for any use.
  • Implant
    FDA-approvedApproved as Scenesse for erythropoietic protoporphyriaSupplied as an implant placed by a certified provider, for a rare condition where sunlight causes severe pain. It is not approved for tanning.
  • Route
    Under the skin (or implant)
  • Checked
    July 2026

What has happened recently

Scenesse is approved for erythropoietic protoporphyria, a rare condition where sunlight causes severe pain. It is supplied as an implant, not as a vial you reconstitute.

You can compare this against the whole library, or read how to check a seller.


Guides for this compound

Sources

  • Pharmacy Times, FDA approval of Scenesse(2019)
    FDA approval of Scenesse for a rare light-sensitivity disorder.
  • FDA prescribing information, SCENESSE (afamelanotide) implant for subcutaneous use, revised August 2024(2024)
    Melanotan I is an approved drug, and reading its label is the fastest way to see how far the approved product is from what people buy. It is not an injection. SCENESSE is a 16 mg bioresorbable rod, 1.7 cm long and 1.45 mm across, inserted under the skin above the hip bone with a specific cannula by a clinician trained by the manufacturer, once every two months. The approved use is narrow: increasing pain-free light exposure in adults with erythropoietic protoporphyria, a rare disorder in which sunlight causes severe pain. Tanning is the mechanism, not the indication. The trial results are modest and worth quoting exactly. In the 93-subject study, subjects on the drug spent a median 64.1 hours in direct sunlight without pain over 180 days against 40.5 on vehicle. In the 74-subject study, the median was 6.0 hours over 270 days against 0.75. Safety comes from 244 subjects, 125 on the drug: implant site reactions in 21% against 10%, nausea 19% against 14%, skin hyperpigmentation 4% against none. Two warnings deserve carrying across to anyone using this off-label. Serious hypersensitivity including anaphylaxis has been reported after approval, which is why the August 2024 revision changed the contraindications. And because the drug darkens existing moles and freckles, the label recommends a full-body skin examination twice a year. Pharmacokinetics come from 12 healthy adults, with an apparent half-life around 15 hours from the implant. No carcinogenicity study has been conducted.

Last reviewed 22 July 2026

Beyond these, 146 records are indexed. Browse the records