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Save B32SP High&Low Molecule HA+Succine Acid
Save B32SP combines hyaluronic acid with 3% succinic acid to visibly rejuvenate aging hands. Its fast-acting formula instantly boosts glow (+29.6% luminosity in 30 minutes) while stimulating long-term collagen growth (+42% in clinical trials). Ideal for sun-damaged skin and volume loss, results last up to 6 months.
$62.00
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 4% | $59.52 |
| 10-19 | 8% | $57.04 |
| 20-Unlimited | 10% | $55.80 |
Save B32SP High&Low Molecule HA+Succinic Acid
Save B32SP combines 3% Succinic Acid (JCRD-certified mitochondrial ATPase activator, +217% activity) with dual-weight hyaluronic acid for cellular-level rejuvenation. Clinical data (n=120) demonstrates 42% increased collagen synthesis in fibroblasts, specifically formulated for hand volume restoration and photoaging reversal. Complies with ISO 13485:2016 medical device standards.
Metabolic Activation
Succinic acid inhibits MMP-1 activity by 68.3% while boosting ATP production 2.17x baseline.
Synergistic Release
HA-Succinate complex ensures pH 7.4-controlled release over 72 hours.
Instant Refinement
29.6% immediate skin luminosity improvement (Cutometer® MPA580 verified).
Core Technology
- Smart Release® nanosphere technology with PLGA carriers
- Precision particle sizing (20-50μm D90 distribution) for mid-dermal delivery
- Dual-phase viscosity modulation (G’ 250-300Pa at 25℃)
Packaging Specifications
Contents: 1.2ml/syringe × 8 units/box
Needles: 25G sharp needles (individually sealed)
Closure: EPFR rubber stopper (≥20 punctures leakage-free)
Storage: 2-8°C protected from light. Do not freeze.
Shelf Life: 18 months unopened
Clinical Protocols
Hand Augmentation
Fan technique: 10 injection points (0.05ml/point)
Depth Control
Deep dermal-subcutaneous junction (30° needle angle)
Contraindications
Avoid concurrent vitamin C derivatives (pH incompatibility risk)
Important Notice
Individual results may vary based on tissue characteristics and injection technique. CFDA adverse reaction rate: <0.33% (2023 data).
For use only by licensed practitioners with Class III implantable device certification (NMPA Registration: 2023345XXXX).
Post-treatment: Avoid radiofrequency devices for 48 hours. Maintain cold chain during transport (2-8°C).
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