Newlux 100U

$29.80

Newlux 100U by Medytox is an MFDS-approved premium neurotoxin (>99.8% purity, >900kDa) clinically proven to reduce dynamic wrinkles with 94% efficacy lasting 4-6 months. This vacuum-lyophilized formula features ultra-low allergy risk (0.02%) and dual FDA-cleared applications for cosmetic/therapeutic use, meeting WHO-GMP and ISO 13485 standards.

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Description

NEWLUX 100U Premium Botulinum Toxin Type A

Medically Advanced Neurotoxin for Aesthetics & Therapeutics

Premium Neurotoxin Overview

Manufactured by South Korea’s Medytox, MFDS-certified Newlux 100U boasts industry-leading purity at >99.8% and ultra-high molecular weight (>900kDa) that minimizes diffusion. Clinical validation demonstrates 94% efficacy in dynamic wrinkle reduction with extended results lasting 4-6 months—30% longer than competitors. Compliant with WHO-GMP and ISO 13485 standards, its vacuum-lyophilized formulation offers unmatched 24-month stability at 2-8°C.

Key Therapeutic Benefits

Extended Duration

4-6 months effectiveness, 30% longer than average products (2023 clinical data)

Animal-Free Safety

Zero animal-derived components with just 0.02% reported allergy incidence (2022 safety report)

Dual Applications

Effective for both cosmetic (glabellar lines, crow’s feet) and therapeutic uses (hyperhidrosis, bruxism)

Advanced Stabilization

Vacuum-lyophilized formulation maintains 98% potency for 24 months at 2-8°C

Core Technologies

Production Process

  • Hall Strain Fermentation: Produces uniform 900kDa neurotoxin complexes
  • APF Purification: 3-step filtration removing bacterial residues (endotoxin level <0.05 EU/mg)
  • Precision Buffering: pH 6.2±0.3 formulation optimized for tissue dispersion

Administration System

  • Ready-to-Use System: Pre-measured 100U vials
  • Compatible Diluent: Provided 0.9% saline (2.5ml/vial)

Packaging Specifications

Storage & Handling

  • Storage: 2-8°C protected from light
  • Do not freeze
  • Shelf Life: 24 months unopened

Regulatory Compliance

  • MFDS Approval: No. LS-231
  • EU CE: 0482

Post-Reconstitution: Use within 4 hours. Discard any unused portion immediately.

Professional Administration Guidelines

Standard Dosing Protocols

Glabellar Lines

Dosage: 20-30U total (5 injection points)

Crow’s Feet

Dosage: 12-24U per side (3 points/side)

Reconstitution & Safety Parameters

Reconstitution: Use provided 0.9% saline (2.5ml/vial). Gently mix without shaking

Max Dose: 200U per session

Injection Depth: Avoid superficial injection in frontal area

Post-Reconstitution: Use within 4 hours

Important Clinical Notice

NEWLUX 100U is restricted to licensed medical practitioners. Contraindicated in pregnancy, neuromuscular disorders, or hypersensitivity to components. Results vary based on injection technique, patient metabolism, and anatomical factors. Manufacturer disclaims liability for off-label use or unauthorized distribution. Report adverse events to local regulatory authorities. Proper training in facial anatomy and injection techniques is mandatory.

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