Botox® 100 Units | Allergan Aesthetics (OnabotulinumtoxinA)
Short Description
The global gold standard in neuromodulator therapy, Botox® by Allergan Aesthetics (an AbbVie company) is the most researched and clinically validated Botulinum Toxin Type A formulation in aesthetic medicine. Engineered with a proprietary 900 kDa molecular complex, it provides unmatched precision, predictable localized diffusion, and peer-reviewed safety for dynamic facial line correction and therapeutic indications.
Detailed Description
Botox® (OnabotulinumtoxinA) is the benchmark injectable neuromodulator worldwide, supported by more than 30 years of clinical application and over 500 peer-reviewed scientific articles. Produced via proprietary fermentation and purification protocols, each vial contains a uniform, vacuum-dried formulation of Clostridium botulinum type A neurotoxin complexed with protective hemagglutinin and non-toxic non-hemagglutinin proteins.
By cleaving SNAP-25 within the presynaptic nerve terminal, Botox® temporarily impedes the exocytosis of acetylcholine at the neuromuscular junction. This controlled neuro-relaxation smooths hyperdynamic lines and contours the facial architecture while maintaining predictable dosing profiles and natural tissue dynamics.
Treatment Areas & Indications
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Upper Facial Aesthetics:
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Moderate-to-severe glabellar lines (frown lines between the brows)
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Lateral canthal lines (crow’s feet)
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Horizontal forehead rhytids
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Mid-to-Lower Face & Neck Sculpting:
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Masseter muscle hypertrophy (jawline contouring and bruxism management)
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Depressor Anguli Oris (DAO) modulation to correct downturned mouth corners
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Mentalis smoothing (chin dimpling / “peau d’orange”)
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Platysmal bands and jawline definition (Nefertiti Lift)
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Bunny lines (transverse nasal lines)
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Therapeutic & Dermatology Applications:
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Severe primary axillary and palmar hyperhidrosis
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Chronic migraine prophylaxis
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Blepharospasm and hemifacial spasm
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Key Clinical Advantages
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The 900 kDa Standard: The heavy molecular weight complex provides a controlled, localized field of effect with minimal lateral migration, protecting adjacent non-target musculature.
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Batch-to-Batch Uniformity: Rigorous biological potency assays ensure consistent therapeutic potency across every manufactured lot.
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Unmatched Clinical Backing: Holds extensive approvals from the US FDA, EMA, and global health authorities across both aesthetic and medical specialties.
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Reliable Longevity: Clinical results typically become evident within 3 to 5 days, reaching peak clinical expression at 14 days, with sustained clinical efficacy lasting 3 to 4+ months.
Technical Specifications
| Parameter | Specification |
| Active Substance | OnabotulinumtoxinA (Clostridium botulinum Type A Neurotoxin Complex) |
| Molecular Complex Weight | Approximately 900 kDa |
| Nominal Strength | 100 Allergan Units (IU) per vial |
| Formulation | Sterile vacuum-dried powder in a transparent glass vial |
| Excipients | 0.5 mg Human Albumin, 0.9 mg Sodium Chloride |
| Manufacturer | Allergan Pharmaceuticals Ireland / AbbVie Inc. |
| Reconstitution Agent | Sterile, preservative-free 0.9% Sodium Chloride Injection, USP | Storage Specifications | Store unopened at 2°C to 8°C or frozen at or below -5°C. |
| Administer within 24 hours of reconstitution (kept refrigerated at 2°C to 8°C) | Regulatory Status | Prescription Only (Rx) — Strictly for Licensed Medical Practitioners |
Professional Advisory: Botox® is an authentic medical-grade pharmaceutical intended exclusively for licensed dermatologists, plastic surgeons, maxillofacial surgeons, and qualified aesthetic practitioners. Not authorized for direct consumer sales or self-administration.









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