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Liztox 200u
Liztox 200U — 200-unit pack of freeze-dried Clostridium botulinum toxin type A Cost-efficient Korean botulinum for high-volume practice. For licensed healthcare professionals only.
$48.50
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 3% | $47.05 |
| 10-19 | 5% | $46.08 |
| 20-Unlimited | 8% | $44.62 |
Liztox 200U — Type A Botulinum Toxin
What it is
Liztox 200U is the larger pack format of Huons Biopharma’s BioPure-extracted botulinum — same formulation, same BioPure Extraction Process as Liztox 100U, but with 200 units per vial. Designed for high-volume practices, multi-area cosmetic protocols, and therapeutic indications requiring 100+ unit doses, while maintaining Liztox’s low-immunogenicity positioning.
What makes it distinctive
Liztox 200U combines Huons Biopharma’s BioPure-extracted formulation with 200U pack economics. Positioned for high-volume practices serving long-term repeat patients where antibody formation risk matters. Positioned for high-volume practices serving long-term repeat patients where antibody formation risk matters.
Why the 200U Liztox pack suits long-term repeat practices
Long-term repeat patients face theoretical risk of neutralizing antibody formation from accumulated exposure to inactive complexing proteins in botulinum products. Liztox’s BioPure Extraction Process minimizes inactive protein content per dose. The 200U pack format supports high-volume use within the 12-hour reconstituted shelf life constraint specific to Liztox. Typical 200U scenarios: 2–3 patients full upper face per single-vial session; combined cosmetic full-face (glabellar 20U + crow’s feet 24U + masseter 50U per side); bilateral axillary hyperhidrosis (100U per axilla = 200U full vial).
Approved & off-label indications
Multi-area cosmetic combinations (glabellar + crow’s feet + masseter)
Bilateral masseter hypertrophy (jaw slimming)
Multi-patient single-session use (2-3 patients per vial)
Severe primary axillary hyperhidrosis bilateral (100U per axilla)
Long-term repeat patients (low-immunogenicity advantage)
Cervical dystonia therapeutic doses (150–200U)
Body contouring (calf, deltoid hypertrophy)
High-volume routine cosmetic protocols
Technical specifications
Detail for clinical, regulatory, and shipping reference.
| Active Ingredient | Clostridium botulinum toxin type A complex |
| Strain | proprietary working strain (Huons Biopharma) |
| Molecular Complex | 900 kDa complex · 150 kDa neurotoxin core |
| Units per vial | 200 units |
| Form | Lyophilized white powder (freeze-dried) |
| Excipients | Human serum albumin + sodium chloride (200U scaling) |
| Manufacturer | Huons Biopharma |
| Origin | Pangyo, South Korea |
| Approvals | Manufactured by Huons Biopharma in Korea |
| Onset / Duration | ~day 3 onset · peak day 14 · 3–5 months duration |
| Reconstitution | Sterile preservative-free 0.9% saline |
| Storage | Store at 2–8 °C, protect from light, do not freeze. |
| Reconstituted shelf life | 24 hours at 2–8 °C |
| Shelf life (unopened) | 36 months from manufacture |
| Intended use | Licensed medical professionals only |
Frequently Asked Questions
Is Liztox 200U the same formulation as Liztox 100U?
Yes — identical Huons Biopharma BioPure Extraction Process and working strain. Only the unit count per vial differs: 200 units versus 100.
What’s the per-unit cost compared to Liztox 100U?
The 200U pack offers approximately 18% per-unit savings over the 100U pack. The cost advantage holds if the reconstituted product is used within the 12-hour Liztox-specific shelf life.
Why does Liztox have a 12-hour reconstituted shelf life vs 24-hour for others?
Huons Biopharma’s official IFU specifies 12-hour reconstituted use rather than the 24-hour window typical of other Korean botulinums. Practices using Liztox 200U should plan to complete all treatments within 12 hours of single-vial reconstitution.
Is Liztox 200U FDA-approved?
Liztox is not FDA-approved in the United States. Same regulatory status as Liztox 100U.
When does Liztox 200U make most sense vs Botulax 200U?
Both are 200U Korean botulinums. Choose Liztox 200U if you serve long-term repeat patients where lower-immunogenicity matters or you can complete reconstituted vials within 12 hours. Choose Botulax 200U if you prefer the 24-hour reconstituted window or want Korea’s #1 brand recognition.
Can I reconstitute Liztox 200U and split across multiple patients?
Yes, provided all patients are treated within 12 hours of reconstitution (Liztox-specific window) and the reconstituted solution is kept refrigerated at 2–8 °C between draws. Each patient should be treated with fresh sterile syringe from the multi-dose vial. Discard residual product after 12 hours.
How do I verify Liztox 200U authenticity?
Same checks as Liztox 100U: (1) Huons Biopharma branding on outer carton with Pangyo reference; (2) batch number matching between box and vial; (3) ‘200U’ clearly printed on labeling; (4) BioPure Extraction reference; (5) intact tamper-evident vial seal; (6) visible white lyophilized powder cake in the larger 200U vial.
Related Products
Other botulinum toxin products from MJS Medicals — different manufacturers, formulations, and price points.
Browse all botulinum toxin products at MJS Medicals.
Safety
This product-specific: Liztox 200U 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: June 2026 · Source verification: Manufacturer documentation
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