Melanotan 1

FDA-approved drug

Also known as: MT-1, afamelanotide analog

Melanotan 1 is a synthetic alpha-MSH analog related to afamelanotide, but an online MT-1 vial is not the FDA-approved SCENESSE implant.

Melanotan 1 quick facts

Category
Cosmetic
Evidence level
FDA-approved drug
Common research sizes
10 mg
Cheapest current price per mg
$2.25/mg at NextGen Peptides
Last reviewed
September 17, 2026
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Storage
-20°C
After reconstitution
No validated universal window
On this page

What it is

Melanotan 1 was the development name for a synthetic analog of alpha-melanocyte-stimulating hormone. The pharmaceutical form, afamelanotide, is now delivered as the prescription SCENESSE implant for adults with erythropoietic protoporphyria.

Retail Melanotan 1 powder is not SCENESSE. It lacks the approved implant formulation, controlled release, manufacturing standards, and medical indication. It should also not be confused with Melanotan 2, a different analog with broader receptor activity.

What people research it for

Approved EPP treatment

Human studies

SCENESSE increases pain-free light exposure in adults with erythropoietic protoporphyria.

Increased pigmentation

Human studies

Melanocortin-1 receptor activation increases eumelanin and darkens skin.

Vitiligo research

Early human data

Afamelanotide plus narrowband UVB has shown repigmentation signals in selected trials.

Retail tanning vials are not approved

Preclinical / theorized

No online MT-1 vial is interchangeable with the licensed implant.

How it works

Afamelanotide activates the melanocortin-1 receptor on melanocytes, increasing eumelanin production. Eumelanin darkens skin and helps absorb ultraviolet radiation.

The approved implant releases afamelanotide over time to increase pain-free light exposure in erythropoietic protoporphyria. More pigment does not eliminate ultraviolet damage or replace sun protection and skin-cancer screening.

What the research actually shows

Two randomized trials in erythropoietic protoporphyria compared afamelanotide implants with placebo. Participants receiving afamelanotide had more pain-free time in direct sunlight, though the absolute trial endpoints and regional studies differed.

Those studies used a sterile, controlled-release implant administered by trained professionals. They did not test loose lyophilized Melanotan 1 powder or cosmetic self-tanning use.

FDA approved SCENESSE in 2019 to increase pain-free light exposure in adults with a history of phototoxic reactions from erythropoietic protoporphyria. The label requires trained administration and skin monitoring.

Vitiligo trials have paired afamelanotide implants with narrowband ultraviolet B treatment. Some repigmentation signals were reported, but this is a separate medical research setting and not approval for cosmetic tanning.

Case reports and reviews of unlicensed melanotan products describe changing moles and concern about melanoma detection. They cannot prove causation, but they reinforce the need for skin surveillance.

There is no controlled evidence that unapproved MT-1 vials are a safe substitute for sunscreen, reduce skin-cancer risk, or match SCENESSE exposure.

Handling & storage

Storage at a glance

FDA label
Lyophilized
-20°C
Supplier guidance for research powder only. This is not SCENESSE.
Reconstituted
No validated universal window
The approved drug is a solid implant and is not reconstituted.
Light
Keep any product in its original packaging and follow product-specific instructions.
Room temperature
SCENESSE is labeled for refrigerated storage at 2 to 8°C.
Reconstitution
Follow product-specific instructions
Do not apply vial instructions to the approved implant.

Basis: FDA label. Sources: FDA SCENESSE prescribing information, American Peptides Melanotan 1 technical page

The FDA label says the sealed SCENESSE implant should be refrigerated at 2 to 8°C. It is a sterile solid implant and is not reconstituted.

A retail Melanotan 1 powder is a different product. Supplier freezer guidance for that powder must not be presented as the label for SCENESSE, and neither product should be improvised into another form.

Safety & cautions

The SCENESSE label warns about generalized pigmentation and darkening of existing nevi and freckles. It calls for full-body skin examinations before and during treatment. Common adverse reactions include implant-site reactions, nausea, fatigue, dizziness, and headache.

Unapproved powders add uncertain identity, strength, sterility, and pharmacokinetics. Pigment changes can complicate mole monitoring, and tanning does not make ultraviolet exposure safe.

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Frequently asked questions

Is Melanotan 1 the same as SCENESSE?

They share the afamelanotide lineage, but an online MT-1 vial is not the FDA-approved controlled-release SCENESSE implant.

Is Melanotan 1 FDA approved for tanning?

No. SCENESSE is approved for a rare phototoxicity disorder, not cosmetic tanning.

Is Melanotan 1 the same as Melanotan 2?

No. They are different melanocortin analogs with different receptor profiles.

Does darker skin from afamelanotide prevent sun damage?

No. Pigmentation does not replace sunscreen, protective clothing, or skin examinations.

Why are mole checks important?

Afamelanotide can darken existing nevi and freckles, and unlicensed melanotan use can complicate recognition of changing lesions.

How is SCENESSE stored?

The FDA label specifies refrigeration at 2 to 8°C for the sealed implant. Research powder is a different product with different instructions.

Sources

Last reviewed September 17, 2026. This guide is educational and research-focused, not medical advice. Melanotan 1 products referenced on PeptidePub are sold by third parties as materials for laboratory research use only, not for human or animal consumption.

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