Home>Injections>Botulinum Toxins>ReNTox™ – Clostridium Botulinum Toxin Type A (100iu)

ReNTox™ – Clostridium Botulinum Toxin Type A (100iu)

£116.00 £99.00

ReNTox™ 100 units is an innovative drug (botulinum toxin) type A premium class, developed by the South Korean company Pharma Research Bio.

Description

ReNTox™ 100 units is an innovative drug (botulinum toxin) type A premium class, developed by the South Korean company Pharma Research Bio.

This drug has gained great popularity in clinics of South Korea and Japan due to several advantages:

1) 3D effect: the patient feels the result already for 3 days, the duration of action is 6-8 months

2) Composition: the improved formula of the preparation does not contain: proteins, albumin, gelatin, compared with other similar drugs.

3) Diffusion: has the least diffusion among all botulinum toxins currently known.

 

Indications

– correction of facial wrinkles.
– blepharospasm;
– hemifacial spasm;
– cervical dystonia (spastic torticollis);
– focal spasticity of the wrist and hand in stroke patients;
– paralytic strabismus (squint);
– local muscle spasm in cerebral palsy in children aged 2 years and older;
CONTRAINDICATIONS, COMPLICATIONS, POSSIBLE SIDE EFFECTS:

  • hypersensitivity to the components of the composition;
  • pregnancy and lactation;
  • inflammatory processes on the skin in the target area;
  • bleeding disorders;
  • herpes, as well as any infectious and chronic systemic diseases in the acute stage;
  • fever;
  • diabetes;
  • oncological diseases;
  • pronounced hernial protrusions on the lower and upper eyelids;
  • myasthenia gravis (Myasthenia Gravis) – an autoimmune disease that causes chronic muscle fatigue syndrome;
  • age before 18 and after 65 years.

Injections of the drug should be carried out by a qualified doctor who has undergone a training course.

Manufacturer: Pharma Research Bio, South Korea.

 

[Composition]

Each 1 vial contains

  • Clostridium botulinum toxin type A (in house) 100 Units
  • Human serum albumin (EP) 0.5 mg
  • Sodium chloride (EP) 0.9 mg

[Description]

It appears as a lyophilized white powder for injection in a colorless transparent vial and should become colorless transparent liquid when the diluent (normal saline) is added.

[Indication]

Temporary improvement in the appearance of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity in adult patients aged between 18 and 65

[Packing unit]

1 vial

[Storage]

The unopened lyophilized vial should be stored in a refrigerator (2-8°C)

[Shelf life]

36 months from the manufacturing date

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