Kaimax 100UI
Clostridium botulinum toxin type A · 100 units · lyophilised powder, single-dose vial. Manufactured by JETEMA Co, Ltd, South Korea.
Original price was: $58.90.$46.90Current price is: $46.90.
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Kaimax 100UI is a 99.8%-pure botulinum toxin type A from JETEMA, built on a low-protein formula to reduce resistance risk over repeated use. It’s used for glabellar lines, forehead lines, crow’s feet, and masseter (jaw) treatment.
Professional use only. This product is intended for administration by licensed healthcare practitioners trained in the relevant anatomy and injection technique. By ordering you confirm you are authorised to purchase and handle products of this class in your jurisdiction. Availability and permitted use vary by country — please verify local regulations before ordering.
In accordance with applicable U.S. FDA regulations, this product is not available for purchase or shipment to U.S. addresses through this website. Customers in the United States should obtain botulinum toxin products through appropriately licensed and authorized U.S. distribution channels. A valid medical license or registration certificate is required to process any product-related claim.
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JETEMA's botulinum toxin type A, with a 36-month shelf life
Kaimax is a botulinum toxin type A product from JETEMA Co, Ltd, supplied as a sterile lyophilised powder in a single 100-unit vial and reconstituted with preservative-free 0.9% sodium chloride before use.
The specification worth noting is the 36-month shelf life from manufacture. That is at the longer end for this category, and it matters commercially rather than clinically: a longer dating window gives more room to hold stock without racing an expiry date, which is useful if you order in volume or supply irregularly scheduled treatment programmes.
JETEMA is a Korean manufacturer better known in the dermal filler market, with Kaimax as its botulinum toxin line. In handling terms it is a conventional lyophilised toxin — stored at 2–8 °C, reconstituted by the practitioner, dilution chosen to suit the treatment area.
At the longer end for this category, which gives more room to hold stock without racing an expiry date.
Botulinum toxin type A with human serum albumin and sodium chloride — no unusual handling or storage.
Supplied as a powder, so concentration is chosen at the bench to suit the treatment area.
JETEMA Co, Ltd, a Korean producer also active in the dermal filler market.
Why practitioners choose Kaimax 100UI
A 36-month shelf life from manufacture gives more flexibility when ordering in volume or holding stock for scheduled treatment programmes.
Reconstitutes and stores like any lyophilised toxin, so it slots into an existing workflow without retraining.
Supplied as a powder rather than a solution, so concentration is set at the bench to suit the treatment area.
100 U and 200 U share the same formulation, so vial size can be matched to session volume.
Aesthetic & therapeutic applications
Areas commonly treated with this product. Approval status differs between markets — always work from the prescribing information registered in the country where you practise.
Corrugator and procerus activity produces the vertical lines between the brows. It is the standard first treatment for a new patient because the muscles are large, the landmarks are reliable, and the result is easy for the patient to see for themselves at a two-week review.
Lines at the outer eye produced by orbicularis oculi activity. Widely treated in aesthetic practice; whether it is an approved indication for this product depends on your market.
Horizontal lines from frontalis activity, typically treated with small doses across several points. A practitioner decision within local regulations.
Not an indication as such, but the longer dating window makes this product easier to hold for programmes booked months in advance, where stock has to sit before it is used.
Botulinum toxin products are prescription-only medicines. Any use outside the indications approved in your jurisdiction is a clinical decision made by the treating practitioner under their own professional judgement and local regulatory framework. Korea Filler Experts supplies the product; nothing here should be read as a recommendation to treat any medical condition.
What is inside Kaimax 100UI
| Active substance | Clostridium botulinum toxin type A |
| Strength | 100 Units per vial |
| Stabiliser | Human serum albumin, 0.5 mg |
| Tonicity agent | Sodium chloride, 0.9 mg |
| Pharmaceutical form | Lyophilised powder for solution for injection |
| Shelf life | 36 months from date of manufacture |
| Diluent | Preservative-free 0.9% sodium chloride injection (not supplied) |
| Container | Single-use glass vial |
| Route | Intramuscular injection |
| Manufacturer | JETEMA Co, Ltd, South Korea |
| Regulatory class | Prescription-only medicine (professional use) |
Reading the carton
Before you accept a delivery, check four things:
- The lot / batch number on the carton matches the number printed on the vial.
- The expiry date — with a 36-month shelf life, fresh stock should carry a long dating window. Ask us before ordering if you need a specific one.
- The seal is intact and the vial has not been disturbed.
- The carton arrived cold, with the coolant pack still chilled.
Vial looks empty? The contents are freeze-dried under vacuum, so the powder forms a thin film that is hard to see against the glass. This is expected and is not a sign of a short fill.
What each component does
- Botulinum toxin type A — the active substance. It temporarily reduces the release of acetylcholine at the neuromuscular junction, lowering activity in the injected muscle.
- Human serum albumin — stabilises the toxin protein through freeze-drying, storage and reconstitution. This is a human blood derivative; if a patient raises that specifically, an albumin-free product such as Coretox or Innotox is the alternative.
- Sodium chloride — brings the reconstituted solution to a tonicity suitable for injection.
How to prepare and use Kaimax 100UI
Reference information for licensed practitioners. Reconstitution and administration must follow the prescribing information approved in your market and your own clinical governance procedures.
Step by step
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Inspect the vial
Check the label, lot number and expiry date, and confirm the seal is intact.
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Prepare the diluent
Draw the required volume of preservative-free 0.9% sodium chloride injection into a sterile syringe.
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Disinfect the stopper
Wipe the exposed rubber stopper with an alcohol swab and allow it to dry.
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Introduce the diluent slowly
Insert the needle at an angle and let the vacuum draw the saline in. Direct the stream against the vial wall rather than onto the powder.
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Mix gently
Rotate the vial slowly to dissolve the cake. Do not shake vigorously. The solution should be clear, colourless and free of particulates.
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Record and use promptly
Note the reconstitution date and time on the vial, store at 2–8 °C, and use within the period stated in your approved prescribing information.
Dilution reference
| Diluent added | Units per 0.1 mL | Total volume |
|---|---|---|
| 1.0 mL | 10.0 U | 1.0 mL |
| 2.0 mL | 5.0 U | 2.0 mL |
| 2.5 mL | 4.0 U | 2.5 mL |
| 4.0 mL | 2.5 U | 4.0 mL |
| 5.0 mL | 2.0 U | 5.0 mL |
Administration notes
Materials needed: preservative-free 0.9% sterile saline, a sterile syringe with a fine-gauge needle, gloves and alcohol swabs. None of these are supplied with the vial.
Note that the long shelf life applies to the unopened vial. Once reconstituted, the in-use period is the same as any other toxin and is set by your approved prescribing information.
- Units of botulinum toxin are product-specific. Do not convert or substitute units between brands.
- Dose per site, total dose and injection technique must follow the prescribing information approved in your market.
- Draw reconstituted product immediately before injection.
- Treatment intervals should not be shortened below the minimum stated in the prescribing information.
After treatment
- Avoid rubbing or massaging the treated area for at least 24 hours
- Stay upright and avoid lying down for 4 to 6 hours
- Avoid strenuous exercise for 24 to 48 hours
- Avoid saunas, hot tubs and excessive sun exposure for at least 24 hours
- Mild redness, swelling or bruising can occur and usually settles within a few days
Storing and handling Kaimax 100UI
Store refrigerated at 2–8 °C in the original carton, protected from light. Do not freeze. Shelf life is 36 months from manufacture — work to the printed expiry date rather than assuming the full term remains.
Keep at 2–8 °C and use within the period stated in your approved prescribing information. The long unopened shelf life does not extend the in-use period. Single-patient use only.
Transfer stock into a monitored medical refrigerator on arrival and keep a temperature log. If a shipment arrives warm, photograph the packaging and contact us before putting it into clinical service.
Do not use the vial if the powder is discoloured, if the reconstituted solution is cloudy or contains particles, if the expiry date has passed, or if the cold chain is known to have been broken. Dispose of unused product and used vials as clinical waste in line with local requirements.
What's included with Kaimax 100UI
Diluent (0.9% sodium chloride injection), syringes and needles are not supplied with this product and must be sourced separately.
Kaimax 100UI — frequently asked questions
What is Kaimax 100UI?
Kaimax 100UI is a botulinum toxin type A product manufactured by JETEMA Co, Ltd. in South Korea. It is supplied as a sterile freeze-dried powder in a single 100-unit vial and reconstituted with preservative-free 0.9% sodium chloride before injection by a licensed practitioner.
What does the 36-month shelf life actually mean for me?
It applies to the unopened vial, measured from the date of manufacture. A longer dating window gives more room to hold stock without racing an expiry — useful if you order in volume or run irregularly scheduled treatment programmes.
It does not extend the in-use period after reconstitution, which is the same as any other toxin.
How much shelf life will my stock actually have?
That depends on when the batch was made, not on the 36-month term. We do not dispatch stock with less than six months remaining unless you have specifically agreed to it, and we can confirm the exact expiry date of your allocated stock before dispatch if you ask.
Why does the vial look empty?
The contents are freeze-dried under vacuum, so 100 units of active substance form a very thin, almost transparent film in the vial. This is normal for lyophilised toxins and is not a sign of a short fill. The powder becomes obvious once saline is introduced.
How should I dilute a 100 U vial?
Dilution volume is chosen by the practitioner. Adding 2.5 mL of preservative-free 0.9% sodium chloride gives 4 units per 0.1 mL, which is a commonly used concentration; the reference table above lists other volumes.
Should I order the 100 U or 200 U vial?
Both share the same formulation, so the choice is about session volume. The 100 U vial suits face-focused lists; the 200 U vial reduces how many you open when treating larger muscle groups. Reconstituted product is single-patient use, so size the vial to the session.
Can I substitute Kaimax units for another brand's units?
No. Units of botulinum toxin are specific to each product and are not interchangeable between brands. Dosing must be taken from the prescribing information for the product in your hand.
What happens if my shipment arrives warm?
Do not use it. Photograph the outer box, the insulated liner, the coolant packs and the vial carton, and contact us the same day with your order number. We will review the cold-chain evidence and arrange a replacement where the failure occurred in transit.
Who is allowed to buy this product?
Botulinum toxin is a prescription-only medicine. Purchase and use are restricted to licensed healthcare professionals qualified to prescribe or administer injectable prescription medicines in their jurisdiction, with appropriate training in the relevant anatomy and injection technique. We do not sell to consumers.
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