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[FDA] Nabota 200u
[FDA] Nabota 200u
[FDA] Nabota 200u
$95.00/ea
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[FDA] Nabota 200u

[FDA] Nabota 200u

Regular price $95.00 USD
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Botulinum toxin type A Nabota is indicated for the temporary treatment of glabellar lines associated with cardboard lines and / or decreased abdominal muscle activity in adult patients less than 65 years of age. Botulinum toxin type A (Nabota) is indicated for the treatment of focal armpit hyperhidrosis.

 

Description

Botulinum toxin type A (Nabota) is indicated for the temporary improvement in the appearance of the upper respiratory tract (forehead lines, crow's feet and forehead lines) in adults. Botulinum toxin type A (Nabota) is indicated for the prevention of headaches in adults with chronic migraine.

Botulinum toxin type A (Nabota) is indicated for the treatment of urinary incontinence due to neurogenic detrusor overactivity, e.g., spinal cord injury (SCI) or multiple sclerosis (MI) in adults.

 

INDICATION

Temporary improvement in the appearance of moderate to severe glabellar lines associated with ripple and / or lower abdominal activity in adult patients 
Treatment of upper limb spasticity in adult patients 
Transient improvement in the appearance of moderate to severe lateral angular lines associated with ocular activity in adult patients 
Treatment of dystonia-related blepharospasm in adult patients 
HI Pure TM technology

Composition: volume - 200 units

 

The package includes a glass ampoule in which the powder is placed under pressure. Sometimes the ampoule may seem empty. For use, dilute the powder in the ampoule with saline. For 100 units, add 2.5 ml of saline, for 200 units - 5 ml of saline.

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