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Botulax 300ui
Botulax 300U — Hugel Pharma’s 300-unit pack (launched 2024) of freeze-dried botulinum toxin type A. MFDS (KFDA) approved. Its active FDA-approved as Letybo (2024). Highest single-vial unit count in the Hugel family. For licensed healthcare professionals only.
$65.00
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 3% | $63.05 |
| 10-19 | 5% | $61.75 |
| 20-Unlimited | 8% | $59.80 |
Botulax 300U — Hugel Largest-Pack Format
How is the 300U reconstituted?
300U is typically reconstituted with 7.5 mL preservative-free 0.9% saline for 4U/0.1 mL dilution (same concentration as 100U with 2.5 mL or 200U with 5 mL). Higher concentration protocols (e.g. 5 mL → 6U/0.1 mL) are possible for therapeutic large-muscle work. Use within 24 hours at 2–8 °C.
Is 300U overkill for a single patient?
Typically yes — single-patient cosmetic treatment rarely exceeds 100U. The 300U pack is designed for multi-patient sessions or therapeutic indications. For single-patient practices, Botulax 100U is more appropriate.
Can I split the 300U across multiple session days?
No. Once reconstituted, Botulax must be used within 24 hours at 2–8 °C. Unused reconstituted product must be discarded after 24 hours. The 300U pack is operationally suited to sustained high-volume practices that can complete the full vial within the day.
How do I verify authenticity?
Same as smaller Botulax packs: (1) Hugel branding and KOSDAQ 145020 reference; (2) batch number matching between box and vial; (3) ‘300U’ clearly printed on labeling; (4) intact tamper-evident vial seal; (5) visible white lyophilized powder cake in the larger 300U vial format.
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Safety
This product-specific: Botulax 300U carries the same class-wide botulinum toxin warnings as all Type A products including potential distant toxin spread, neuromuscular junction disorder contraindications, and pregnancy/lactation contraindication. Always aspirate before injection; maintain emergency airway management equipment.
Botulinum toxin Type A is a prescription medical product for licensed healthcare professionals only. Contraindicated in neuromuscular junction disorders (myasthenia gravis, Lambert-Eaton, ALS); known hypersensitivity to botulinum toxin or excipients; pregnancy / breastfeeding; active local infection; concurrent aminoglycoside / anticholinesterase / curare-like drugs. Class-wide warning: rare distant toxin spread possible (symptoms hours-to-weeks post-injection). Maintain emergency airway management equipment and epinephrine.
Last reviewed: May 2026 · Source verification: Manufacturer official documentation · Multi-distributor cross-check
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