Innotox is Medytox’s ready-to-use liquid botulinum toxin type A: the first liquid-formulation toxin, so it needs no reconstitution. It is albumin-free, formulated with L-methionine, polysorbate 20 and phosphate-buffered saline, supplied as a 100 U vial, and registered with Korea’s MFDS. Medytox has no FDA-approved toxin, so no FDA status is claimed. Potency units are product-specific. Professional use only.
What is Innotox?
Innotox is Medytox’s ready-to-use liquid botulinum toxin type A — introduced as the first liquid-formulation botulinum toxin, so it needs no reconstitution. It is albumin-free, formulated with L-methionine, polysorbate 20 and phosphate-buffered saline, and supplied as a 100 U vial. Because it arrives pre-mixed, it removes the saline-dilution step before injection. Potency units are specific to this product and are not interchangeable with other botulinum toxin products.
How does Innotox differ from freeze-dried toxins?
Unlike the freeze-dried Botulax, Coretox and Meditoxin, Innotox is a ready-to-use liquid that skips reconstitution, and it is albumin-free. It is also a Medytox product, sitting beside Coretox and Meditoxin in the Medytox range.
| Innotox | Medytox · ready-to-use liquid · albumin-free · 50/100 U |
|---|---|
| Coretox | Medytox · free of complexing proteins · freeze-dried · 100 U |
| Botulax | Hugel · complex-type · freeze-dried · 100/200/300 U |
What do clinics use Innotox for?
Clinics select Innotox for facial expression-line work where a ready-to-use liquid is wanted to avoid the reconstitution step. Dosing and technique are product-specific and decided by the treating clinician per the manufacturer’s labelling; units are not interchangeable with other toxins.
Commonly selected for
- Clinics wanting a ready-to-use liquid toxin
- Workflows that avoid saline reconstitution
- Practices preferring an albumin-free formulation
- Aesthetic expression-line protocols
How is Innotox supplied?
One 100 U ready-to-use liquid vial; no reconstitution is required. Follow the manufacturer’s handling instructions.
Reviewed against publicly available manufacturer information. Indications, dosing and technique are product-specific per the manufacturer’s labeling and are decided by the treating clinician.
Specifications
| Brand | Innotox (Medytox) |
|---|---|
| Manufacturer | Medytox Inc. (South Korea) |
| Origin | South Korea |
| Active | Botulinum toxin type A (100 U), liquid |
| Composition | Clostridium botulinum type A toxin in a ready-to-use liquid; albumin-free, with L-methionine, polysorbate 20 and phosphate-buffered saline |
| Units | 100 U |
| Format | 100 U ready-to-use liquid vial |
| Areas | Facial expression lines (aesthetic use) |
| Delivery | Ready to use — no reconstitution; inject intramuscularly per the practitioner’s protocol |
| Regulatory | Registered with Korea’s MFDS. Its maker, Medytox, does not have an FDA-approved botulinum toxin product, so no FDA status is claimed. |
| Administration | Injectable — by a qualified medical professional only |
| Storage & handling | Store refrigerated (2–8 °C) per the manufacturer’s instructions. |
Frequently asked questions
Does Innotox need reconstitution?
No. Innotox is a ready-to-use liquid botulinum toxin type A; it is injected directly without saline dilution.
Is Innotox albumin-free?
Yes. It is formulated without albumin, using L-methionine, polysorbate 20 and phosphate-buffered saline.
Is Innotox FDA-approved?
No. It is registered with Korea’s MFDS. Medytox does not have an FDA-approved botulinum toxin product.
How is it supplied?
As one 100 U ready-to-use liquid vial, with no reconstitution required.
Are its units interchangeable with other toxins?
No. Potency units are specific to this product and are not converted 1:1 to other botulinum toxin products.