
Oxytocin.
Nonapeptide hormone — bonding, intimacy and prosocial neuromodulation.
Build your bag, then either book a consultation (an EU-licensed physician reviews your file — anything declined is refunded) or upload an existing Rx at checkout.
- ✓Magistral preparation — Directive 2001/83/EC Art. 5(1).
- ✓Patient-named prescription only — dispensed against a valid Rx.
- ✓EU-GMP Annex 1 Grade A/B cleanroom compounding.
- ✓Cold-chain shipping across EU/EEA — 2–5 working days.
About Oxytocin.
Oxytocin is a 9-amino-acid neurohypophyseal hormone with both peripheral (uterine contraction, lactation) and central (social bonding, stress buffering) effects. Licensed pharmaceutical preparations are widely available for obstetric use.
Off-label magistral use targets the prosocial and intimacy-supporting effects, generally at low doses given intranasally or by injection.
Oxytocin binds the oxytocin receptor (OXTR) on many cell types. Centrally, it modulates amygdala reactivity (dampening threat response) and ventral-tegmental dopamine release (enhancing reward of social interaction). Peripherally, it acts on uterine smooth muscle and mammary myoepithelium.
Subcutaneous injection, typically 5–10 IU per dose. Intranasal administration is more common for prosocial protocols.
Your physician sets the prescription. This is descriptive information, not a self-administration guide.
Lyophilised: store at 2–8 °C, protect from light. Once reconstituted: 2–8 °C, use within 30 days. Do not freeze.
- INN / Name
- Oxytocin
- Form
- Lyophilised vial · subcutaneous injection
- Strength
- 5mg vial
- Manufacturing
- EU-GMP Annex 1 · Grade A/B
- Endotoxins
- European Pharmacopoeia 2.6.14 · LAL assay
- Identity & purity
- HPLC + MS · > 98%
- Cold chain
- Validated 2–8 °C, monitored end-to-end
- Regulatory basis
- Directive 2001/83/EC · Article 5(1)
2–5 working days
EU / EEA cold-chain delivery, 2–8 °C monitored end-to-end with digital temperature log. Tracking link sent on dispatch.
Magistral preparation
Patient-named preparation under Directive 2001/83/EC Article 5(1). Dispensed exclusively against a valid EU prescription.
EU prescription recognition
Prescriptions written in one EU member state are recognised in others under Directive 2011/24/EU on cross-border healthcare.
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