20 mL Hyaluronic Acid Gel
A confirmed 20 mL hyaluronic acid gel format in a graduated plastic syringe with 20, 22 and 24 mg/mL concentration options.
Public portfolio parameters
Current B2B portfolio baseline for initial format review.
- Net volume
- 20.0 mL per syringe
- Hyaluronic acid concentration
- 20 mg/mL / 22 mg/mL / 24 mg/mL
- Presentation
- Graduated plastic syringe
- 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.
20 mL Plastic-Syringe Configuration
The GuangLong 20 mL format moves the gel range into a dedicated large plastic-syringe presentation. The syringe barrel, graduation scale and extended plunger assembly are configured for the stated 20 mL net volume.
Confirmed Public Parameters
- Net volume: 20.0 mL per syringe
- Hyaluronic acid concentrations: 20 mg/mL, 22 mg/mL or 24 mg/mL
- Primary presentation: Graduated plastic syringe
- Manufacturing entity: GuangLong
- B2B coordination: Innovision Bio
Three-Concentration Project Review
The selected concentration is confirmed before packaging and labeling development. Project alignment covers syringe material, connector, graduation layout, plunger length, protective tray, foil pouch, carton and destination-market labeling.
Information Confirmed Per Project
Cross-linking status, final formulation, component references, sterilization records and market-specific documentation remain part of the qualified project review. The public presentation does not constitute an IFU or registration.
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.