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NABOTA 100U

$57.70

Nabota® Botulinum Toxin Type A (100 Units) is a South Korean–manufactured muscle relaxant formulated from Clostridium botulinum neurotoxin. It targets areas of excessive muscle tone or dynamic facial expression to temporarily reduce…

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Description

Nabota® Botulinum Toxin Type A (100 Units) is a South Korean–manufactured muscle relaxant formulated from Clostridium botulinum neurotoxin. It targets areas of excessive muscle tone or dynamic facial expression to temporarily reduce lines and wrinkles.

Key Benefits

  • Smoothes dynamic wrinkles for a rejuvenated appearance
  • Reduces excessive sweating in underarms, palms, and soles
  • Delivers aesthetic effects lasting 6–9 months
  • Provides therapeutic relief for chronic migraines and involuntary muscle spasms

Features & Specifications

  • Active Ingredient: Botulinum toxin type A (100 Units per vial)
  • Diluent: 0.9% Sodium Chloride
  • Dilution Guide (per 0.1 mL):

    • 1.0 mL → 10 U
    • 2.0 mL → 5 U
    • 2.5 mL → 4 U
    • 4.0 mL → 2.5 U
    • 8.0 mL → 1.25 U
  • Package: 1 vial (100 Units)
  • Needle: 30 gauge recommended
  • Aesthetic Duration: 6–9 months
  • Shelf Life: 36 months from the manufacture date

Storage

Store at 2~8℃.

Usage & Administration

Cosmetic Indications

  • Forehead lines, glabellar (frown) lines, crow’s feet
  • Nasolabial folds, perioral wrinkles, brow wrinkles

Therapeutic Indications

  • Chronic migraine prophylaxis (head and neck injection sites)
  • Hyperhidrosis (underarms, palms, soles)
  • Muscle spasm disorders (e.g., cervical dystonia, blepharospasm)

Dosage Guidelines

  • Cosmetic sessions typically use 20–60 Units, adjusted per treatment area
  • Higher doses may be needed for therapeutic applications
  • Administer only by qualified healthcare professionals

Mechanism of Action

Nabota® binds to presynaptic nerve terminals and blocks acetylcholine release at the neuromuscular junction, preventing muscle contraction and reducing local muscle activity or sweat secretion.

Safety & Contraindications

Common Side Effects: Localized injection-site pain, bruising, headache, and temporary adjacent muscle weakness

Rare Reactions: Allergic responses

Precautions

  • Review patient history for neuromuscular disorders or hypersensitivity
  • Use with caution in patients with impaired respiratory function

Injection Interval: 2–3 treatment sessions per year, as clinically indicated

Call to Action

Experience smoother lines and targeted relief with professional Nabota® treatments. Contact your certified provider to schedule a consultation and tailor a treatment plan to your needs.

Shipping & Origin

  • Manufactured in: Korea
  • Shipping: Available globally for international distribution

NABOTA® is a high-purity Botulinum Toxin Type A formulation developed by Daewoong Pharmaceuticals. FDA-approved and backed by multiple clinical trials, it delivers reliable, temporary smoothing of moderate to severe dynamic wrinkles.

Composition

  • Clostridium botulinum toxin type A: 200 U
  • Human serum albumin: 0.5 mg
  • Sodium chloride: 0.9 mg

Appearance & Reconstitution

Supplied as a white-to-light-yellow lyophilisate in a clear vial. Reconstitute with sterile, preservative-free 0.9 % saline to achieve 4 U/0.1 mL (200 U/5 mL). Gently swirl; avoid agitation—label with date/time and use within 24 hours.

Mechanism of Action

NABOTA® inhibits acetylcholine release at neuromuscular junctions, producing localized muscle relaxation that softens expression lines and relieves hyperactive muscle conditions.

Indications

Aesthetic

  • Temporary improvement of moderate to severe glabellar lines
  • Forehead lines
  • Crow’s feet
  • Periorbital and perioral wrinkles

Therapeutic

  • Chronic migraine prevention
  • Neurogenic detrusor overactivity (urinary incontinence)
  • Axillary hyperhidrosis

Administration

Inject intramuscularly using a 30–33 G needle. Tailor dose and injection sites to individual anatomy and treatment goals. Typical interval between treatments is 3–6 months.

Storage & Shelf Life

Store unopened vials at 2–8 °C; do not freeze. Maintain aseptic handling of the reconstituted product. Shelf life: 36 months from manufacture.

Safety & Precautions

Administer only by licensed professionals. Inspect the solution for particulate matter and discoloration before use. Contraindicated in patients with known hypersensitivity to any component. Common adverse events include injection-site discomfort, localized weakness, and transient ptosis. Serious systemic effects are rare but warrant prompt medical attention.

Disclaimer:
Bruno Dermal Fillerth products are strictly intended for use by licensed medical and aesthetic professionals. Not suitable for self-administration or use by untrained individuals.

Additional information

Weight 0.7 lbs

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