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Melanotan-1 UV Protection Protocol: Clinical vs Recreational Comparison

Clinical (EPP photoprotection) 0.16mg/kg daily × 14 days 0.16mg/kg every 60 days Maximum pigmentation at 4–6 weeks, sustained with bimonthly dosing Erythropoietic protoporphyria, polymorphous light eruption, solar urticaria Nausea (15%), injection site reactio

This comparison does not assign a generated winner or score.

  • Clinical (EPP photoprotection)
  • 0.16mg/kg daily × 14 days
  • 0.16mg/kg every 60 days
  • Maximum pigmentation at 4–6 weeks, sustained with bimonthly dosing
  • Erythropoietic protoporphyria, polymorphous light eruption, solar urticaria
  • Nausea (15%), injection site reaction (8%), headache (5%)
  • FDA-approved under brand name Scenesse for EPP. Highest evidence base for photoprotection efficacy
  • Recreational (aesthetic tanning)
  • 0.1–0.12mg/kg daily × 10–14 days
  • 0.08–0.12mg/kg 2–3× weekly
  • Visible tanning at 7–10 days, peak at 3–4 weeks
  • Pre-vacation tanning, phototype I–II skin baseline before UV exposure
  • Similar to clinical but dose-dependent. Higher maintenance doses increase nausea risk
  • Not FDA-approved for cosmetic use. Protocol derived from off-label clinical data
  • Minimal Maintenance
  • 0.1mg/kg daily × 7 days
  • 0.08mg/kg once weekly
  • Light pigmentation at 10–14 days, requires UV co-exposure to deepen
  • Individuals seeking subtle tan without frequent injections
  • Lower nausea incidence due to reduced cumulative dose
  • Insufficient for true photoprotection. Best suited for users with phototype III–IV baseline
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