Community / anecdotal. Community / anecdotal — no regulatory basis. Not medical advice.
Typical — reference only
Loading ~100-250 mcg/day, then ~500-1000 mcg 1-2x/week maintenance SC
Worked reconstitution example
10 mg vial + 2 mL BAC = 5 mg/mL; 500 mcg = 10 U on U-100. Intranasal absorption is unpredictable - mcg figures don't translate.
Titration
Start low to gauge nausea/BP
Units are not milligrams. mg-vs-mcg confusion drives documented 5–1000× overdoses — always recompute for your own vial (use the calculator →).
Removal from Category 2 ≠ legal to compound ≠ FDA-approved. Removal != legal/approved. Banned as a medicine in the UK; Schedule 9 (prohibited) in Australia (Feb 2026).
StatusBanned / prohibited
503A bulksNot on the bulks list
Category 2 (2026)Removed from Category 2 ~22 Apr 2026; on the ~Feb 2027 PCAC
PCAC review~2027-02
WADANot listed
03Evidence — the honest read
Bhuman trials
Early-phase human + small tanning studies; NO approval. Evidence is largely evidence of HARM (case reports).
Contraindications
- Melanoma / dysplastic nevi / skin-cancer historyhard stop
- Uncontrolled hypertension / known CVDhard stop
- History of priapism / sickle cell
- Pregnancyhard stop
Key interactions
- PDE5 inhibitors (HARD_STOP/avoid; severe hypotension/syncope + priapism)
Serious signals
- Priapism (urologic emergency)
- PRES; rhabdomyolysis; renal infarction (case reports)
- Mole darkening / new nevi / melanoma - complicates surveillance
Monitoring
Regular dermatologic mole surveillance; baseline BP.
01TGA Schedule 9 2026; case reports
+PepTrack research dossier — iterations 1–4, 584 de-duplicated sources, adversarially verified.
Not medical or legal advice. Educational / harm-reduction reference. Regulatory and dosing claims in this field move monthly — re-verify against primary sources (FDA docket FDA-2025-N-6895, DailyMed, ClinicalTrials.gov) before acting.
Last reviewed — 2026-06-13 · confidence: medium