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PINE BOTTLE Skin Contouring Solution

$65.00

Clinically-formulated biopharmaceutical solution combining 98% natural active ingredients: phosphatidylcholine (82% purity), bromelain (1200 GDU/g), and riboflavin. Proven to enhance skin elasticity by 37% in clinical observations while enabling safe adipocyte metabolism. Delivers visible contour refinement within 3-day post-treatment cycles when administered by certified professionals.

Quantity discounts
Quantity Discount Price
5-9 3% $63.05
10-19 5% $61.75
20-Unlimited 8% $59.80
SKU: 26080904a203-9f16-46b0-92de-5c427392d15b Categories: ,

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INIBO 100U BOTULINUM TOXIN TYPE A

Purified neurotoxin complex (900 kDa) produced via Clostridium botulinum fermentation. Utilizes proprietary vacuum-drying technology ensuring >99.8% structural integrity and minimizing protein aggregation. Formulated with Human Serum Albumin (HSA) to prevent adherence to glass and maintain long-term stability. KMFDS-certified (KLH No.2023-MD-0451). Strictly distributed for licensed clinical administration.

Composition per

Active: Clostridium Botulinum Toxin Type A (100 Units)
Stabilizer: Human Serum Albumin (0.5 mg)
Tonicity Adjuster: Sodium Chloride (0.9 mg)
Appearance: White freeze-dried powder

Pharmacodynamics

Onset of Action: 48-72 hours post-injection
Peak Efficacy: 14 days post-administration
Clinical Duration: 3-6 months
Diffusion Radius: Controlled (< 3mm standard dilution)

Reconstitution Protocol & Standard Dosing

Reconstitute exclusively with sterile, preservative-free 0.9% Sodium Chloride. Gentle swirling is required; strictly prohibit aggressive agitation to prevent peptide bond denaturation. Administer via 30G-32G microneedle.

Dilution Ratio:
2.5ml Saline = 4.0U / 0.1ml
1.25ml Saline = 8.0U / 0.1ml

Target Topography:
Glabellar Complex: 20-30U
Lateral Canthal Lines: 12-24U
Frontalis: 10-20U

Storage & Contraindications

Unopened must be refrigerated at 2-8°C (35.6-46.4°F). Shelf life is 36 months from manufacturing date. Reconstituted solution must be utilized within 24 hours. Absolute contraindications include established hypersensitivity, active infection at injection site, and neuromuscular junction disorders (e.g., Myasthenia Gravis, Lambert-Eaton syndrome, ALS). Not evaluated for systemic administration.

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