100 mL Hyaluronic Acid Gel
A confirmed 100 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
- 100.0 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.
100 mL Dual-Presentation Configuration
The GuangLong 100 mL format is the largest confirmed public volume in the current gel range. It is presented through a graduated plastic syringe or a sealed vial, with no bag configuration included.
Confirmed Public Parameters
- Net volume: 100.0 mL
- Hyaluronic acid concentrations: 20 mg/mL, 22 mg/mL or 24 mg/mL
- Presentation options: Graduated plastic syringe or vial
- Bag presentation: Not included
- Manufacturing entity: GuangLong
- B2B coordination: Innovision Bio
Large-Format Packaging Review
The plastic-syringe option requires alignment on barrel material, graduation sequence, connector, long-plunger geometry and transit protection. The vial option requires a confirmed vessel, closure, seal, graduation layout and secondary carton. The selected format and concentration must remain consistent across the project record.
Information Confirmed Per Project
Cross-linking status, final formulation, component references, sterilization records and target-market documentation are reviewed for the actual B2B configuration. This public page is not an IFU, registration or final release specification.
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.