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For professional use only.
Manufacturer: Humedix Co. Ltd
Active Substance(s): BOTULINUM TOXIN TYPE A
Strength: 100u
Pack Size: 1 x 100u Vial
Liztox® Inj. is a type A botulinum toxin, the product composition provides effective skin flattering through the smoothing of middle-to-deep wrinkles. Liztox is a highly-purified clostridium botulinum toxin type A for correction and preventive care of mimic wrinkles. Due to inhibition of signaling between muscles and motor nerves, the product acts as a myorelaxant and is used for the control of dynamic wrinkles. The levelling effect of Liztox is reached by the correction of both, small and deep wrinkles. Applying regularly, the product effectively prevents formation of new folds. In addition, Liztox may be used for the treatment of increased diaphoresis via injections at the perspiratory gland localization (palms, axillas, foot).
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INFORMATION
LIZTOX Botulinum Toxin Key Features and Benefits
LIZTOX® 100u is a prescription botulinum toxin type A product used to temporarily improve moderate to severe facial wrinkles. Manufactured by Huons Biopharma Co., Ltd, Liztox comes as a powder that must be diluted with saline to create a clear, transparent solution for injection. The Liztox correction treatment includes the primary features:
- Effective Wrinkle Treatment: This Addresses glabellar lines (frown lines) and lateral canthal lines (crow’s feet) with precision.
- Durable Results: Effects last approximately 3–4 months.
- Proven Efficacy: Demonstrated in clinical trials with high patient satisfaction.
- Ease of Administration: Optimized for precision using a 30–33 gauge needle.
This aesthetics needle or botulinum toxin offers two Liztox vials: 100 Units and 200 Units. Medical professionals can select which of the vials or Liztox powder can effectively address the patient’s concerns.
Mixing LIZTOX – Reconstitution Process and Dilution Chart
When mixing Liztox, this botulinum toxin requires specific reconstitution to ensure safe and effective use. The process involves diluting the lyophilized powder with 0.9% sodium chloride injection.
Moreover, in Liztox mixing, the appropriate dilution ratio should be tailored to align with the healthcare professional’s and patient’s specific preferences and requirements. This individualized approach ensures optimal efficacy and safety for the intended treatment. Typically, the dilution chart is as follows:
- 1.0 mL diluent: 20 Units /0.1 mL concentration.
- 2.0 mL diluent: 10 Units /0.1 mL concentration.
- 4.0 mL diluent: 5 Units /0.1 mL concentration.
- 8.0 mL diluent: 2.5 Units /0.1 mL concentration.
Key Instructions:
- Add the diluent slowly to mix and avoid foaming.
- Administer within 24 hours of reconstitution.
- Store the diluted product at 2–8°C.
LIZTOX® 100u Storage Information
Unopened and unused Liztox must be refrigerated at 2–8°C. After reconstitution, the solution should also be refrigerated and used within 24 hours. Proper handling of Liztox vials and medical waste disposal procedures, such as diluted hypochlorite for decontamination, is recommended.
LIZTOX Botulinum Toxin Treatment Areas
LIZTOX® is an FDA-approved aesthetics for the treatment of:
- Glabellar Lines: Targets the corrugator and procerus muscles.
- Lateral Canthal Lines: Addresses the orbicularis oculi muscle for crow’s feet.
Injection sites include:
- Five points in the glabellar region (0.1 mL per site, totaling 20 U).
- Six points per eye for lateral canthal lines (0.1 mL per site, totaling 24 U).
LIZTOX® 100u Dosing for Different Indications
Dosing Recommendations:
- Glabellar Lines: 20 U per treatment session, diluted to 100 U/2.5 mL.
- Lateral Canthal Lines: 24 U per treatment session, diluted similarly.
LIZTOX Botulinum Side Effects and Precautions
Liztox botulinum has undergone rigorous testing, but typical reactions can occur. These may differ from one patient to another, but the potential Liztox side effects include:
Common Liztox Side Effects:
- Injection Site Reactions: Redness, swelling, and bruising.
- Systemic Reactions: Nasopharyngitis (5.19%), headaches (0.74%).
Rare and Serious Adverse Events:
- Muscle Weakness and Ptosis: Avoid injections near sensitive structures.
- Neurological Effects: Potential risk in patients with underlying conditions like myasthenia gravis.
Precautions
- Avoid use in patients with hypersensitivity to any components.
- Exercise caution when patients are taking muscle relaxants or aminoglycoside antibiotics.
LIZTOX Botulinum Toxin Aftercare
These post-treatment guidelines are crucial to ensure patient safety and the product’s maximum efficacy. Licensed and experienced medical professionals must inform patients that adhering to the post-treatment care instructions can help them achieve their treatment goals.
- Avoid makeup application, UV exposure, and extreme temperatures for 24 hours.
- Patients should avoid rubbing or massaging the treatment area to prevent toxin migration.
LIZTOX® 100u Drug Interactions
Drug interactions can enhance systemic or localized effects:
- Contraindicated Medications: Aminoglycosides, spectinomycin, and polymyxin.
- Caution with Anticholinergics: May amplify systemic effects.
LIZTOX Botulinum Toxin Key Features and Benefits
LIZTOX® 100u is a prescription botulinum toxin type A product used to temporarily improve moderate to severe facial wrinkles. Manufactured by Huons Biopharma Co., Ltd, Liztox comes as a powder that must be diluted with saline to create a clear, transparent solution for injection. The Liztox correction treatment includes the primary features:
- Effective Wrinkle Treatment: This Addresses glabellar lines (frown lines) and lateral canthal lines (crow’s feet) with precision.
- Durable Results: Effects last approximately 3–4 months.
- Proven Efficacy: Demonstrated in clinical trials with high patient satisfaction.
- Ease of Administration: Optimized for precision using a 30–33 gauge needle.
This aesthetics needle or botulinum toxin offers two Liztox vials: 100 Units and 200 Units. Medical professionals can select which of the vials or Liztox powder can effectively address the patient’s concerns.
Mixing LIZTOX – Reconstitution Process and Dilution Chart
When mixing Liztox, this botulinum toxin requires specific reconstitution to ensure safe and effective use. The process involves diluting the lyophilized powder with 0.9% sodium chloride injection.
Moreover, in Liztox mixing, the appropriate dilution ratio should be tailored to align with the healthcare professional’s and patient’s specific preferences and requirements. This individualized approach ensures optimal efficacy and safety for the intended treatment. Typically, the dilution chart is as follows:
- 1.0 mL diluent: 20 Units /0.1 mL concentration.
- 2.0 mL diluent: 10 Units /0.1 mL concentration.
- 4.0 mL diluent: 5 Units /0.1 mL concentration.
- 8.0 mL diluent: 2.5 Units /0.1 mL concentration.
Key Instructions:
- Add the diluent slowly to mix and avoid foaming.
- Administer within 24 hours of reconstitution.
- Store the diluted product at 2–8°C.
LIZTOX® 100u Storage Information
Unopened and unused Liztox must be refrigerated at 2–8°C. After reconstitution, the solution should also be refrigerated and used within 24 hours. Proper handling of Liztox vials and medical waste disposal procedures, such as diluted hypochlorite for decontamination, is recommended.
LIZTOX Botulinum Toxin Treatment Areas
LIZTOX® is an FDA-approved aesthetics for the treatment of:
- Glabellar Lines: Targets the corrugator and procerus muscles.
- Lateral Canthal Lines: Addresses the orbicularis oculi muscle for crow’s feet.
Injection sites include:
- Five points in the glabellar region (0.1 mL per site, totaling 20 U).
- Six points per eye for lateral canthal lines (0.1 mL per site, totaling 24 U).
LIZTOX® 100u Dosing for Different Indications
Dosing Recommendations:
- Glabellar Lines: 20 U per treatment session, diluted to 100 U/2.5 mL.
- Lateral Canthal Lines: 24 U per treatment session, diluted similarly.
LIZTOX Botulinum Side Effects and Precautions
Liztox botulinum has undergone rigorous testing, but typical reactions can occur. These may differ from one patient to another, but the potential Liztox side effects include:
Common Liztox Side Effects:
- Injection Site Reactions: Redness, swelling, and bruising.
- Systemic Reactions: Nasopharyngitis (5.19%), headaches (0.74%).
Rare and Serious Adverse Events:
- Muscle Weakness and Ptosis: Avoid injections near sensitive structures.
- Neurological Effects: Potential risk in patients with underlying conditions like myasthenia gravis.
Precautions
- Avoid use in patients with hypersensitivity to any components.
- Exercise caution when patients are taking muscle relaxants or aminoglycoside antibiotics.
LIZTOX Botulinum Toxin Aftercare
These post-treatment guidelines are crucial to ensure patient safety and the product’s maximum efficacy. Licensed and experienced medical professionals must inform patients that adhering to the post-treatment care instructions can help them achieve their treatment goals.
- Avoid makeup application, UV exposure, and extreme temperatures for 24 hours.
- Patients should avoid rubbing or massaging the treatment area to prevent toxin migration.
LIZTOX® 100u Drug Interactions
Drug interactions can enhance systemic or localized effects:
- Contraindicated Medications: Aminoglycosides, spectinomycin, and polymyxin.
- Caution with Anticholinergics: May amplify systemic effects.
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