Medically Reviewed & Clinical Efficacy Verified | Board-Certified Dermatologist Approved
Professional-Grade Numbing Solution: Neo Pro Cream 450G
Medical-grade 10.56% lidocaine emulsion engineered for clinical dermatological and aesthetic procedures. Utilizes a liposomal delivery system to ensure rapid dermal penetration, providing sustained anesthesia for up to 120 minutes. Optimized for high-frequency laser therapies, microneedling, and extensive dermal pigmentation sessions.
Core Clinical Metrics
Rapid Absorption
15-20 minute initial onset time via liposomal encapsulation.
Sustained Efficacy
90-120 minute peak anesthetic duration post-removal.
Optimal Concentration
10.56% active Lidocaine matrix (45.5g per 450g volume).
Technical Specifications & Pharmacokinetics
Active Ingredient: Lidocaine 10.56%
Formulation Base: Water-in-oil (W/O) pharmaceutical emulsion
Density & pH: 1.5g/cm³ | pH 6.5 – 7.0 (Skin barrier compatible)
Volume/Weight: 450g (Sterile clinical jar)
Storage Protocol: 2°C – 25°C (35°F – 77°F). Strictly avoid UV exposure.
Shelf Life: 24 months (Unopened) | 6 months (Post-opening)
Clinical Application Protocol
1. Dermal Preparation: Degrease and sanitize target epidermis using 70% isopropyl alcohol. Ensure complete dryness.
2. Precise Dosage: Dispense approximately 0.5g per cm². Apply a uniform 1.5mm to 2.0mm opaque layer over the treatment vector.
3. Occlusion Strategy: Apply a non-breathable osmotic film (plastic wrap) to prevent active ingredient evaporation and accelerate thermal absorption. Maintain for 15-25 minutes.
4. Pre-Procedure Removal: Remove film and extract all residual emulsion using sterile gauze. Do not commence dermal puncture or laser application with surface residue present.
Strict Medical Advisory & Contraindications
Authorized for professional administration by licensed aesthetic and medical practitioners only. Strictly contraindicated for patients with documented amide local anesthetic hypersensitivity or severe hepatic impairment.
Systemic Toxicity Warning: Maximum cumulative application area must not exceed 400cm² (approx. 20cm x 20cm) within a 24-hour period. Avoid mucous membrane contact. Transient erythema (localized redness) and minor blanching are standard physiological responses post-application.

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