50 mL Hyaluronic Acid Gel
A confirmed 50 mL hyaluronic acid gel format with plastic-syringe and vial presentations in 20, 22 and 24 mg/mL concentrations.
Public portfolio parameters
Current B2B portfolio baseline for initial format review.
- Net volume
- 50.0 mL
- Hyaluronic acid concentration
- 20 mg/mL / 22 mg/mL / 24 mg/mL
- Presentation
- Graduated plastic syringe or vial
- Cross-linking
- Monophasic (default); biphasic available for qualified B2B projects
- Storage
- Store at 2°C–25°C; protect from light; do not freeze.
- Shelf life
- 24 months
- Manufacturing entity
- GuangLong
Final release specifications, target-market documentation and any use claims remain subject to the qualified project review.
50 mL Dual-Presentation Configuration
The GuangLong 50 mL format is available for B2B review in two distinct presentations: a graduated plastic syringe and a sealed vial. Both formats represent the same stated net volume but require separate component, labeling and secondary-packaging decisions.
Confirmed Public Parameters
- Net volume: 50.0 mL
- Hyaluronic acid concentrations: 20 mg/mL, 22 mg/mL or 24 mg/mL
- Presentation options: Graduated plastic syringe or vial
- Manufacturing entity: GuangLong
- B2B coordination: Innovision Bio
Syringe and Vial Review Paths
The plastic-syringe path covers barrel material, graduation direction, connector, plunger travel and tray protection. The vial path covers vessel material, closure system, graduation layout, seal and carton protection. The selected concentration and presentation are kept consistent across labels and project records.
Information Confirmed Per Project
Cross-linking status, final formulation, component references, sterilization records and destination-market documentation are reviewed for the selected configuration.
Project review
Before requesting project-specific information
A concise brief helps us confirm the right commercial and documentation path for your discussion.
- Identify the target market, responsible entity, and intended professional channel.
- Describe the commercial scope, packaging concept, and indicative project timing.
- State the discussion stage and whether an NDA is already in place.
- Request only the information needed for the current qualified review stage.
Project-specific materials are considered only after qualification and do not represent product approval, registration, or a public technical specification.