1 mL Hyaluronic Acid Gel
A confirmed 1 mL hyaluronic acid gel presentation with a 24 mg/mL concentration, prefilled syringe and two needle components for B2B review.
Public portfolio parameters
Current B2B portfolio baseline for initial format review.
- Net volume
- 1.0 mL per syringe
- Hyaluronic acid concentration
- 24 mg/mL
- Presentation
- Graduated prefilled syringe
- Cross-linking
- Monophasic (default); biphasic available for qualified B2B projects
- Pack components
- Two needle components, molded tray and foil pouch
- 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.
Batch quality reference
Results for the GuangLong 1 mL cross-linked sodium hyaluronate gel batch shown below.
- Appearance
- Colorless, transparent; no visible foreign matter
- Fill volume
- 114% of labelled fill volume (enterprise standard: 90%–120%)
- Crosslinking-agent residue
- 1.1 μg/g (enterprise standard: ≤ 2.0 μg/g)
- Endotoxin
- < 0.5 EU/mL
- Osmotic pressure
- 362 mOsmol/kg
- Sterility
- Sterile
This is a batch-specific Certificate of Analysis reference. It does not represent every batch, concentration or presentation.
1 mL Prefilled-Syringe Configuration
This page presents the confirmed public baseline for the GuangLong 1 mL hyaluronic acid gel format. The primary presentation is a single graduated prefilled syringe with two needle components in a clear tray and foil pouch.
Confirmed Public Parameters
- Net volume: 1.0 mL per syringe
- Hyaluronic acid concentration: 24 mg/mL
- Primary presentation: Graduated prefilled syringe
- Pack components: Two needle components, molded tray and foil pouch
- Manufacturing entity: GuangLong
- B2B coordination: Innovision Bio
B2B Packaging Review
The 1 mL format supports project discussions where a compact single-syringe presentation is required. Needle gauge, component supplier, tray layout, foil-pouch artwork, carton count and labeling language are confirmed against the buyer brief and destination market.
Information Confirmed Per Project
Final product specification, cross-linking status, component references, sterilization records, labeling and applicable market documentation are reviewed for the qualified project. The public image is a representative packaging presentation, not a registration or IFU.
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.