Your Brand Identity
on a Documented Supply Chain
Private label means the product carries your identity while the manufacturing sits under a certified quality management system. What you control is the brand; what you can verify is the supply behind it.
Engineering Anatomy
What carries your branding
A unified physical packaging system. Each layer is engineered to balance visual prestige, sterile integrity, and destination market regulatory compliance.
Sterile & Non-Sterile Zones: Primary glass barrel and stopper undergo moist-heat autoclaving; outer retail box and multi-language IFU are assembled in secondary clean zones.
Prefilled Borosilicate Syringes & Vials
Neutral borosilicate glass engineered for smooth, uniform extrusion force, low friction plunger resistance, and long-term chemical stability.
- 1 ml, 2 ml, 10 ml prefilled glass syringes; 3 ml & 5 ml sterile glass vials
- High-precision silk-screened graduation scale markings & fill lines
- Customized plunger rod colors & matching safety luer-lock tip caps
- Medical chlorobutyl rubber stoppers with terminal steam sterilization
Medical Blister Trays & Tyvek® Lidding
Custom thermoformed rigid blister trays paired with heat-sealed lidding that forms a sterile barrier for clinic field transfer.
- Rigid PET / PVC blister trays with tailored syringe and needle cavities
- Puncture-resistant Tyvek® breathable paper or medical aluminium foil lidding
- High-definition monochrome or full-color branding & LOT/EXP coding on foil
- Fiber-free, clean-peel opening ensuring particulate-free aseptic field entry
Engineered Outer Boxes & Finishes
Folding cartons or rigid drawer boxes built to protect the internal sterile barrier during air transit while establishing brand presentation.
- Tuck-end folding cartons, rigid slide-out drawer boxes, or clamshell structures
- Matte soft-touch lamination, gold/silver hot foil stamping, embossing, spot UV
- Pre-allocated high-contrast white panel for batch LOT, MFG date, and EXP
- Tamper-evident holographic security stickers or void-pattern seals
Multi-Language IFUs & Traceability Stickers
Destination market documentation, clinical instructions, and patient record tracking elements formatted to medical device standards.
- Folded multi-page Instructions For Use (IFU) in target market languages
- Direct syringe barrel wrap labels with declared HA concentration (mg/ml)
- Detachable patient record stickers with matching batch LOT and QR code
- Harmonized ISO 15223-1 medical device symbols (sterile, single-use, storage temp)
Portfolio Availability
Product families open to private label
Standard formulations open to private label branding. Custom concentrations and bespoke mold options are available at higher production tiers.
| Product Family | Delivery Formats | Grades & Custom Scope | Standard MOQ | Turnaround |
|---|---|---|---|---|
| HA Dermal Fillers | 1 ml / 2 ml / 10 ml / 20 ml prefilled syringes | Monophase cross-linked HA gel; custom box finishes, scale printing, multi-language IFU. | 1,000 units | 15–20 days |
| Skin Boosters | 2 ml / 2.5 ml / 3 ml prefilled syringes & sterile vials | Diffuse hydration formulas; packaged as single units or customized multi-syringe clinic kits. | 1,000 units | 15–20 days |
| PN & PDRN Polynucleotides | 2 ml prefilled glass syringe or 3 ml sterile vials | High-purity biocompatible polynucleotides for tissue repair and dermal barrier regeneration. | 1,000 units | 18–22 days |
| Biostimulators (PLLA / CaHA) | Lyophilized powder vials (150 mg / 365 mg / 5 ml) | Controlled microparticle biostimulators; custom vial crimp caps, labels, and rigid cartons. | 1,500 units | 20–25 days |
| Exosome Regenerative Systems | Dual-vial kit (Lyophilized powder + diluent solvent) | High-potency cellular signalers in dual-vial blister presentation with custom logo foil sealing. | 1,000 kits | 18–22 days |
| Targeted Meso Cocktails | 5 ml / 10 ml sterile vials (5–10 vials / box) | Targeted aesthetic mesotherapy solutions supplied in branded physician packs with divider trays. | 1,000 boxes | 15–20 days |
Execution Pipeline
From brand asset to release lot
A linear five-stage production pathway. Each phase generates documented verification before advancing to the next milestone.
Product Selection & Specification Lock
Select base formulation, concentration, volume, and packaging format. We issue a technical feasibility confirmation, price schedule, and MOQ commitment.
Dieline Issuance & Artwork Adaptation
We provide exact 1:1 vector dielines for outer cartons, labels, blister paper, and IFUs. Your design team submits artwork, or our team adapts your assets into compliant print files.
Physical Sample Production & Sign-off
A physical sample set—including finished box finishes, blister seal, syringe scale print, and leaflet—is produced and air-couriered to you for physical sign-off.
Cleanroom Filling, Sterilization & QC
Mass production in Class 10,000 cleanrooms under ISO 13485:2016. Syringe filling, terminal steam sterilization, in-process viscosity & extrusion testing, and batch lot coding.
Batch Release & Air Transport Dispatch
Final inspection, secondary packaging assembly, tamper sealing, and export packing. Dispatched via temperature-controlled air freight with full shipping and clearance paperwork.
Verification & Quality
Supply credentials behind your brand
Every production batch carries technical documentation required by clinical buyers and customs authorities.
ISO 13485:2016 Cleanroom Facility
All filling, sealing, and packaging operations are performed under an audited medical device quality management system with Class 10,000 cleanroom controls.
Lot-Specific Certificate of Analysis (CoA)
Every production run includes comprehensive laboratory testing for pH, osmotic pressure, gel viscosity, endotoxin levels (<0.5 EU/ml), and sterility.
Air Transport Non-DG Classification
Official non-dangerous goods classification reports for hyaluronic acid gels ensure unimpeded air cargo clearance through international hubs.
Complete Batch Traceability & Serialization
Individual syringe barrels, blisters, and retail cartons carry unified LOT numbers, manufacturing dates, and expiration coding for full audit trails.
Prepress Guidelines
Artwork & print specifications
All packaging artwork is audited against precision dielines to ensure zero distortion and accurate regulatory pictograms.
Accepted File Formats
Adobe Illustrator (.ai), Vector PDF, or EPS. All typography must be converted to outlines / curves. Embedded images must be at least 300 DPI.
Color Mode & Profiles
CMYK for process printing. Specify exact Pantone (PMS) coated codes for brand-critical spot colors, metallic foils, or screen-printed logos.
Bleed & Safety Margins
Minimum 3 mm bleed on all outer edges of dielines. Keep critical text and barcodes at least 3 mm inside the cutting/creasing lines.
Mandatory Regulatory Zones
We reserve specific zones on the outer box and label for CE/ISO symbols, single-use pictograms, storage temperature ranges, and LOT/EXP stamping.
Buyer Questions
Private label FAQ
Essential operational, legal, and regulatory answers for clinics, medical distributors, and brand founders.
Can I launch a full range of aesthetic products under one unified brand?
Yes. Private label can cover multiple product families—for instance, a 4-grade HA dermal filler collection alongside skin boosters and polynucleotides—with a consistent graphic design system, color-coded packaging tiers, and unified brand language.
Who retains legal ownership of the artwork and packaging designs?
You retain complete ownership of your brand name, trademarks, and artwork assets. We simply adapt your brand design onto our precision packaging dielines and store the production-ready plates for your repeat orders.
What is the standard MOQ for private label versus neutral stock?
For private label (custom retail box, label, blister lidding, and leaflet), standard MOQ is 1,000 to 2,000 units per SKU. If you require neutral stock (standard sterile packaging with unbranded white carton for trial evaluation), MOQ starts from 100 to 500 units.
Can packaging copy and instructions be prepared in multiple languages?
Yes. We frequently produce multilingual packaging and instruction leaflets (IFU) combining English with Spanish, French, Arabic, Russian, or Portuguese. We recommend confirming your destination country’s statutory labelling requirements with your local importer or regulatory agent.
Are sample fees refundable against commercial production orders?
Yes. Physical pre-production sample fees and express courier dispatch costs are credited back in full against your first commercial private label production order.
What technical documentation is provided to support our importer’s registration?
We provide technical specification sheets (TDS), safety data sheets (SDS), Certificates of Analysis (CoA) for sample lots, and manufacturing quality management certificates (ISO 13485 / ISO 9001). Local product registration is executed through your appointed importer or in-country representative.
Request for quotation
Start a private label project
Direct response with technical specifications, tiered quotation and country-specific documentation status.