Dysport 500u

$225

SKU: 100068 Category:

Dysport 500U — Ipsen AbobotulinumtoxinA Korean Import

Active Ingredient
AbobotulinumtoxinA
Units / Vial
500 units
Form
Freeze-dried lyophilized powder
Onset / Duration
2–5 days onset (faster than Botox) · 12–16 weeks therapeutic
Storage
Store at 2–8 °C, protect from light, do not freeze.
Manufacturer
Ipsen
Top Indications
Glabellar lines · Severe primary axillary hyperhidrosis · Cervical dystonia
Approvals & Origin
abobotulinumtoxinA — FDA-approved (2009, Ipsen/Galderma). · CE marked · Korean wholesale import · Origin: France / UK manufacturing

What it is

Dysport 500U is a Western botulinum toxin type A manufactured by Ipsen (France/UK) — distinct from the Korean-manufactured products on this site. The active ingredient AbobotulinumtoxinA is a different molecular variant from OnabotulinumtoxinA (Allergan Botox) and IncobotulinumtoxinA (Xeomin) — Dysport units are NOT interchangeable with Botox units (approximate 2.5:1 ratio). Each vial contains 500 units of freeze-dried Clostridium botulinum type A toxin-haemagglutinin complex, stabilized with 0.125 mg human albumin and 2.5 mg lactose. This Korean-imported version is the same Ipsen formulation sold via Galderma in the US, sourced through Korea’s pharmaceutical wholesale channel with English labeling.

What makes it distinctive

Dysport’s defining clinical feature is wider diffusion compared to Botox or Botulax — ideal for body indications (axillary hyperhidrosis, calf slimming, large-muscle spasticity) and treatments where uniform coverage across a broader area matters. Onset is faster (2–5 days vs typical 3–7 days) and the 500U vial is the largest single-pack format on this site, reducing per-unit cost for high-volume hyperhidrosis or therapeutic practice. Critical caveat: Dysport units are NOT interchangeable with other botulinum products — Dysport:Botox dose ratio is approximately 2.5:1.

Why AbobotulinumtoxinA differs from other botulinum toxins

AbobotulinumtoxinA is a structurally distinct molecular variant — the toxin-haemagglutinin complex sits in the 500–750 kDa range (versus 900 kDa for Onabotulinumtoxin / Allergan Botox / Korean botulinum products). This smaller complex contributes to wider diffusion (broader spread from injection point) and faster onset, but means Dysport units cannot be substituted unit-for-unit with Botox. Standard clinical conversion is approximately Dysport 2.5 units : Botox 1 unit (so 50 Dysport units ≈ 20 Botox units for the same effect). Misapplying Botox dosing to Dysport is a clinically significant error. Additionally, Dysport contains lactose as an excipient — contraindicated in patients with cow’s milk protein allergy.

Approved & off-label indications

Glabellar lines (frown lines) — FDA primary indication
Severe primary axillary hyperhidrosis (wider diffusion advantage)
Cervical dystonia (idiopathic spasmodic torticollis)
Adult upper and lower limb spasticity
Pediatric cerebral palsy spasticity (≥ 2 years)
Blepharospasm and hemifacial spasm
Calf slimming (off-label cosmetic body contouring)
Neurogenic detrusor overactivity

Technical specifications

Detail for clinical, regulatory, and shipping reference.

Active IngredientAbobotulinumtoxinA
StrainClostridium botulinum type A
Molecular Complex500–750 kDa toxin-haemagglutinin complex
Units per vial500 units
FormLyophilized white powder (freeze-dried)
Excipients0.125 mg human albumin + 2.5 mg lactose
ManufacturerIpsen
OriginFrance / UK manufacturing · Korean wholesale import
ApprovalsabobotulinumtoxinA — FDA-approved (2009, Ipsen/Galderma). · CE marked · Korean wholesale import
Onset / Duration2–5 days onset (faster than Botox) · 3–4 months cosmetic · 12–16 weeks therapeutic
ReconstitutionSterile preservative-free 0.9% saline
StorageStore at 2–8 °C, protect from light, do not freeze.
Reconstituted shelf life24 hours at 2–8 °C
Shelf life (unopened)36 months from manufacture (tolerates one 25 °C / 72h excursion)
Intended useLicensed medical professionals only

Frequently Asked Questions

What does ‘Korean-Imported Version’ mean for Dysport?

The product is genuine Dysport manufactured by Ipsen at their licensed facilities in France/UK. ‘Korean-Imported Version’ means the product was imported through Korea’s authorized pharmaceutical wholesale channel and redistributed by MJS Medicals. Sourcing via Korea provides English-labeled product at lower pricing than US/EU direct distribution while maintaining authenticity — the formulation is identical to Dysport sold in the US (via Galderma) and EU.

Are Dysport units the same as Botox units?

No — Dysport (AbobotulinumtoxinA) and Botox (OnabotulinumtoxinA) units are NOT interchangeable. The approximate dose ratio is Dysport:Botox = 2.5:1 to 3:1, meaning 50 Dysport units ≈ 20 Botox units for the same clinical effect. Always refer to Dysport-specific dosing guidelines, not Botox protocols. Misapplying Botox dosing to Dysport is a clinically significant error.

How does Dysport’s wider diffusion affect clinical use?

Wider diffusion is an advantage for body indications where uniform coverage matters: severe primary axillary hyperhidrosis (one vial covers ~2 patients bilaterally), masseter hypertrophy (broader spread reduces nodularity), and calf slimming (large-muscle uniform paralysis). The trade-off is reduced precision in small facial zones — Dysport for crow’s feet requires careful injection technique to avoid spread to lateral orbicularis. Botox or Korean toxins may be preferable for precision facial work.

Why is the lactose excipient important?

Dysport contains 2.5 mg lactose as bulking agent and stabilizer. Patients with cow’s milk protein allergy are contraindicated for Dysport — the lactose can trigger allergic reaction in this specific patient population. This contraindication is unique to Dysport among major botulinum products (most use HSA + NaCl without lactose). Always screen for cow’s milk protein allergy before Dysport administration.

What is Dysport’s storage tolerance?

Standard storage is 2–8 °C refrigerated. Unique to Dysport: unopened vials tolerate a single exposure to temperatures up to 25 °C for up to 72 hours during shipping or temporary handling, after which they must return to 2–8 °C. This temperature excursion tolerance is broader than most botulinum toxins. After reconstitution with 2.5 mL preservative-free 0.9% saline, use within 24 hours at 2–8 °C.

Is Dysport FDA-approved?

abobotulinumtoxinA — FDA-approved (2009, Ipsen/Galderma). This Korean-imported version is the same Ipsen-manufactured product, distributed through Korea’s pharmaceutical wholesale channel. Buyers in the US, EU, and other regulated markets must verify their jurisdiction’s import regulations before purchase.

Why is the 500U vial typical for Dysport?

Dysport’s 500U format reflects its dosing scale — typical aesthetic doses are 50U (glabellar), 100U/axilla (hyperhidrosis), 500U (cervical dystonia starting dose). The 500U vial supports therapeutic indications and bilateral hyperhidrosis in a single vial. For smaller cosmetic-only sessions, the 500U vial provides multi-patient coverage when reconstituted and used within 24 hours.

Related Products

Other botulinum toxin products from MJS Medicals — different manufacturers, formulations, and price points.

Merz · Pure 150 kDa

Xeomin 100U Korean Version

Merz Pharma complexing-protein-free formulation — Korean-imported version.

View product →

AbbVie · Korean Import

Allergan Botox 50U

Global gold-standard botulinum — Korean-imported English-labeled version.

View product →

Daewoong · Vacuum-dried 200U

Nabota 200U

Same Daewoong vacuum-dried HI-PURE™ at 200-unit pack — also FDA-approved as Jeuveau.

View product →

Hugel · Largest Pack

Botulax 300U

Hugel’s 300-unit pack (2024 launch) — lowest per-unit cost for sustained high-volume use.

View product →

Browse all botulinum toxin products at MJS Medicals.

Safety

This product-specific: Dysport 500U 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. Critical: Dysport units are NOT interchangeable with Botox / Korean botulinum units (≈2.5:1 Dysport:Botox ratio). Lactose excipient — contraindicated in cow’s milk protein allergy.

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.

→ Full Botulinum Toxin Safety Information

Last reviewed: May 2026 · Source verification: Manufacturer official documentation · Multi-distributor cross-check

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