Hyaluronic Acid Gel Formats 1–100 mL
Compare representative hyaluronic acid gel formats from 1 mL to 100 mL for qualified B2B packaging and product-configuration discussions.
Hyaluronic Acid Gel Format Overview
The GuangLong hyaluronic acid gel range provides distinct volume and packaging configurations for qualified B2B projects. Innovision Bio coordinates the commercial brief, packaging discussion and target-market review without presenting the public catalogue as an IFU, registration or final technical specification.
Confirmed Format Range
- 1 mL and 2 mL: 24 mg/mL prefilled-syringe formats with two needle components
- 3 mL: 24 mg/mL prefilled-syringe format
- 5 mL: 22 mg/mL or 24 mg/mL prefilled-syringe format
- 10 mL: default cross-linked hyaluronic acid gel configuration in a prefilled syringe
- 20 mL: 20 mg/mL, 22 mg/mL or 24 mg/mL in a graduated plastic syringe
- 50 mL and 100 mL: 20 mg/mL, 22 mg/mL or 24 mg/mL with plastic-syringe and vial presentation options
Prefilled-Syringe Formats for B2B Review
The confirmed 1–5 mL formats are presented as graduated prefilled syringes. Review the public baseline for the 1 mL prefilled syringe, 2 mL prefilled syringe, 3 mL prefilled syringe and 5 mL prefilled syringe before discussing the required presentation, concentration and project scope. The 1 mL and 2 mL formats each include two needle components; the 3 mL and 5 mL formats are presented as syringe-only configurations.
B2B Project Scope
Each discussion confirms the required volume, concentration, presentation format, secondary packaging, labeling language, destination market and documentation path. Manufacturing is attributed to GuangLong; Innovision Bio acts as the B2B commercial and project-coordination contact.
Choosing a Format for Review
Use the related-format links on this page to compare the confirmed public baseline for each volume. Final formulation, component selection, labeling and market-specific documentation remain subject to the actual project review.
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.