Kaimax 100U
$33
Kaimax 100U — Type A Botulinum Toxin
What it is
Kaimax 100U is a Korean botulinum toxin type A manufactured by JETEMA — the same Korean firm behind Toxta and the Starfill HA filler line. Each vial contains 100 units of freeze-dried Clostridium botulinum toxin type A complex, stabilized with 1.0 mg human serum albumin and sodium chloride.
What makes it distinctive
Kaimax’s positioning draws on JETEMA’s growing Korean botulinum portfolio (also Toxta) with competitive formulation. JETEMA emphasizes Korean precision manufacturing standards across their injectable product range. The 1.0 mg HSA content (slightly higher than the 0.5 mg standard) supports stable potency during reconstitution and use.
Why JETEMA’s production matters for botulinum quality
JETEMA is a Korean injectable specialist with growing presence across botulinum toxin (Kaimax, Toxta) and HA filler categories (Starfill, EPTQ S-series). JETEMA’s focused R&D investment in injectable production supports consistent quality across batches. The 1.0 mg HSA excipient (rather than the 0.5 mg standard) provides additional stabilization headroom during reconstitution and short-term in-use storage.
Approved & off-label indications
Technical specifications
Detail for clinical, regulatory, and shipping reference.
| Active Ingredient | Clostridium botulinum toxin type A complex |
| Strain | Clostridium botulinum type A |
| Molecular Complex | 900 kDa |
| Units per vial | 100 units |
| Form | Lyophilized white powder (freeze-dried) |
| Excipients | 1.0 mg human serum albumin + sodium chloride |
| Manufacturer | JETEMA |
| Origin | South Korea |
| Approvals | Manufactured by JETEMA in Korea |
| Onset / Duration | 3–7 days onset · 3–6 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
Kaimax is manufactured by JETEMA, a Korean injectable specialist also known for Toxta (botulinum toxin) and the Starfill / EPTQ S-series HA dermal fillers. JETEMA focuses on injectable aesthetic and therapeutic products across their portfolio.
Both products are JETEMA-manufactured Korean botulinums but use different formulation specifications. Kaimax uses 1.0 mg HSA stabilizer; Toxta uses a different formulation with 0.5 mg HSA. The two lines target different preferences within JETEMA’s botulinum portfolio.
Kaimax is not FDA-approved in the United States. JETEMA manufactures Kaimax at its Korean facility.
Kaimax is positioned in the competitive Korean botulinum tier. Higher purity formulations theoretically reduce immunogenicity risk in patients receiving repeated treatments over years.
JETEMA’s formulation uses 1.0 mg human serum albumin — providing additional protein stabilization during reconstitution and short-term in-use storage. Patients with severe HSA hypersensitivity should consult their healthcare provider.
Per JETEMA literature, duration is 3–6 months in standard cosmetic indications. Onset begins after injection with peak effect at approximately 14 days.
Look for: (1) JETEMA branding on outer carton; (2) batch number matching between box and vial; (3) JETEMA branding reference; (4) intact tamper-evident vial seal; (5) visible white lyophilized powder cake in the vial.
Related Products
Other botulinum toxin products from MJS Medicals — different manufacturers, formulations, and price points.
Kaimax 200U
JETEMA 200-unit pack for multi-area or multi-patient sessions.
View product →
Toxta 100U
JETEMA Korean botulinum .
View product →
Liztox 100U
BioPure Extraction at high-purity — low-immunogenicity Korean alternative.
View product →
Hutox 100U
Korean botulinum from Huons Global (Liztox parent company).
View product →
Browse all botulinum toxin products at MJS Medicals.
Safety
This product-specific: Kaimax 100U 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.
→ Full Botulinum Toxin Safety Information
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