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Allergen Botox 50u
Allergan Botox 50U Korean-imported — genuine OnabotulinumtoxinA manufactured by AbbVie/Allergan. Same global Hall-strain formulation. English-labeled, onabotulinumtoxinA — FDA-approved (Allergan, 2002). For licensed healthcare professionals only.
$115.00
Out of stock
Out of stock
Allergan Botox 50U — Korean-Imported Version
What it is
Allergan Botox 50U is the original FDA-approved botulinum toxin type A — the global gold standard since FDA approval in 2002. The 50U pack format is Korea-specific, suited to single-session glabellar / crow’s-feet protocols where 100U would exceed the session need. This version comes through Korea’s authorized pharmaceutical wholesale channel with English-language labeling — the AbbVie formulation itself is identical to the version sold in North America.
What makes it distinctive
Allergan Botox’s defining strength is two decades of clinical evidence — over 70 countries of regulatory approval and 16+ indications spanning aesthetic and therapeutic medicine. The Hall strain at 900 kDa complex defines the unit reference standard for botulinum toxin dosing globally. When clinicians say ‘Botox units’ as a benchmark, they mean Allergan Botox unit potency. The 50U Korea-specific pack format supports waste-free single-treatment protocols.
Why the global gold standard
Allergan Botox is the original commercial botulinum toxin type A — FDA approved since 2002 for glabellar lines and continuously expanded across 16+ indications including therapeutic uses (chronic migraine, hyperhidrosis, cervical dystonia, blepharospasm, strabismus, spasticity, overactive bladder). The Hall strain at 900 kDa complex sets the unit reference for botulinum dosing globally. This Korean-imported version goes through Korea’s authorized pharmaceutical distribution chain, retaining identical AbbVie manufacturing process and English-language labeling — the only difference from US-direct supply is the distribution route and pricing.
Approved & off-label indications
Glabellar lines (frown lines) — primary FDA indication
Lateral canthal lines (crow’s feet) — FDA approved
Forehead lines
Masseter hypertrophy (jaw slimming)
Severe primary axillary hyperhidrosis
Chronic migraine prophylaxis
Cervical dystonia, blepharospasm, strabismus
Upper and lower limb spasticity
Technical specifications
Detail for clinical, regulatory, and shipping reference.
| Active Ingredient | OnabotulinumtoxinA |
| Strain | Clostridium botulinum type A (Hall strain) |
| Molecular Complex | 900 kDa |
| Units per vial | 50 units |
| Form | Lyophilized white powder (freeze-dried) |
| Excipients | 0.5 mg human serum albumin + 0.9 mg sodium chloride |
| Manufacturer | Allergan |
| Origin | Ireland (manufacturing) · USA brand · Korean wholesale import |
| Approvals | onabotulinumtoxinA — FDA-approved (Allergan, 2002). · CE marked · Korean wholesale import |
| Onset / Duration | 3–5 days onset · 3–4 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
What does ‘Korean-Imported Version’ mean for Allergan Botox?
The product is genuine Allergan Botox manufactured by AbbVie at their licensed facilities. ‘Korean-Imported Version’ means the product was imported through Korea’s authorized pharmaceutical wholesale channel and redistributed by MJS Medicals. Sourcing via Korea bypasses multi-tier US/EU distribution markups while maintaining authenticity and English-language labeling — the formulation is identical to Allergan Botox sold in North America.
Why does the Korean version cost less than US Allergan Botox?
Regional pharmaceutical distribution chains in the US add multiple layers of markup between manufacturer and clinic. The Korean wholesale market provides a more direct route to the same AbbVie-manufactured product, reducing per-vial cost without affecting product authenticity or formulation.
Is the 50U pack smaller than standard?
Yes — Allergan’s standard global vial is 100U. The 50U pack is primarily for single-session protocols (one glabellar treatment, one bilateral crow’s-feet treatment) or precise dosing where 100U would create waste in low-volume practices.
How does Allergan Botox compare to Korean botulinum brands like Botulax or Nabota?
Botulax (Hugel) and Nabota (Daewoong, US name Jeuveau) are clinically non-inferior alternatives at lower price points — both also FDA-approved. Allergan Botox carries the longest clinical track record (2002 FDA approval, 16+ indications), highest brand recognition, and the unit reference standard for botulinum dosing globally. Many practitioners use Allergan for first-time international patients and Korean brands for cost-conscious repeat patients.
How long does Allergan Botox last?
Duration is typically 3–4 months for aesthetic indications. Therapeutic indications follow individual treatment cycles per FDA labeling. Duration may extend slightly with repeated treatments as treated muscles become conditioned.
What’s the storage and reconstitution protocol?
Store unopened vials at 2–8 °C refrigerated. Do not freeze. Reconstitute with sterile preservative-free 0.9% saline per the Allergan IFU. Use reconstituted solution within 24 hours, kept refrigerated.
How do I verify authenticity?
Look for: (1) AbbVie/Allergan holographic seal on outer carton; (2) batch number matching between box and vial; (3) English-language labeling indicating Korean import channel; (4) intact tamper-evident vial seal; (5) recognisable Allergan packaging design with visible white lyophilized powder cake in the 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: Allergan Botox 50U Korean Version is the Korean-imported version of the genuine Western brand — formulation is identical to the US/EU direct supply. Same class-wide botulinum toxin warnings apply including distant toxin spread risk, neuromuscular junction disorder contraindications, and pregnancy/lactation contraindication.
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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Dysport 500u
Dysport 500U Korean-imported — genuine AbobotulinumtoxinA manufactured by Ipsen Pharma (France/UK). English-labeled, Korean wholesale import. ⚠ Units NOT interchangeable with Botox (2.5:1 ratio). abobotulinumtoxinA — FDA-approved (2009, Ipsen/Galderma). CE marked. For licensed healthcare professionals only.
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