Product Design Concept

The ZOEYEN GSH Bio-Cellulose Mask introduces the innovative "fifth-generation cosmetics" concept, moving beyond traditional surface-level products. It utilizes small-molecule active substances inherently found in human cells. By actively penetrating the dermis, these ingredients deliver deep nourishment and inward-outward repair to effectively awaken the skin.

Key Formula and Skincare Applications

Its core formula features high-purity Glutathione (GSH), a vital endogenous tripeptide antioxidant. GSH effectively neutralizes free radicals, minimizes cellular damage, and maintains the activity of vitamins C and E. Blended with premium ingredients like Hyaluronic Acid, MELACLEAR2, and MOIST24, the essence deeply hydrates, brightens, and improves dullness, leaving the skin healthy, radiant, and soft.

Unique Manufacturing Process

To maximize absorption, the mask utilizes organic nano-grade bio-cellulose produced through natural fermentation. With fibers 133 times finer than standard non-woven fabrics, its 3D structure flawlessly adheres to microscopic skin lines, efficiently delivering the essence deep into the skin. This material offers exceptional moisture retention and a perfect fit, allowing users to move freely without slipping. Furthermore, all products are manufactured in GMP-certified facilities and pass rigorous safety tests for guaranteed quality.

Water

Beta-Glucan

1,3 Butylene Glycol

MELACLEAR2

MOIST 24

DERMAWHITE NF LS9410

Urea

ANASENSYL LS9322

Hyaluronic Acid

Methyl Paraben

Allantoin

EDTA

GSH

I. Incoming Material Control

• Documents: COA, SDS, and traceability records are required 7 days pre-production.

• Shelf Life: ≥ 3 months from the material feeding date.

• Storage: Quarantined pending inspection. Requires temp/humidity logs; materials must be sealed and stored ≥ 5 cm from walls and floors.

II. In-Process Control

• Environment & Water: Personnel and goods must use separate routes. Gowning, de-dusting, and sterilization are required. Process water needs RO, deionization, and UV treatment.

• Double Verification: A 2-person verification with documentation is required for material picking, in-process sampling, and packaging.

III. Outbound Inspection

• Testing: Safety inspections must be conducted by TAF or MOHW-certified labs.

• Sampling: ≥ 3 outer cartons checked for correct quantity and serial numbers. ≥ 5 finished boxes checked for appearance and packaging integrity.

IV. Data-Driven Quality Management

• Volume: 23~26 ml of essence per mask.

• Safety Limits: Total plate count < 500 cfu/g. Pathogens (E. coli, P. aeruginosa, S. aureus, C. albicans) and heavy metals (As, Pb, Hg, Cd) must be "Not Detected". Total plasticizers < 100 ppm.

• Monitoring: Retain samples for regular quality testing and maintain continuous post-market supervision.

Testing for heavy metals: (Arsenic, Lead, Mercury, Cadmium)

Plasticizers: (Announced by the Ministry of Health and Welfare / MOHW)

Microorganisms: (Including Total Plate Count, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans)

I. Incoming Material Control

• Doc Review: COA, SDS, and traceability records must be submitted 7 days pre-production and approved before feeding.

• Shelf Life & Release: Materials need ≥3 months of shelf life from the feeding date. They are quarantined and released only upon passing inspection.

II. In-Process Control (Self-Inspection & QA)

• Double Verification: Material picking, sampling, and packaging need 2-person verification with documentation.

• QA Patrol: On-site supervision randomly audits personnel, SOP compliance, and environmental cleanliness.

• 3rd-Party Audits: Manufacturers must fully cooperate with audits by client-appointed third parties.

III. Finished Product Control

• Certified Testing: Safety tests (microbes, heavy metals, plasticizers, pH) must be done by TAF or MOHW-certified labs.

• Sampling & Retention: Both parties retain samples. Inspections check ≥3 cartons for quantity/serial numbers and ≥5 product boxes for visual integrity.

IV. Post-Market Control & Task Force

• Exception Handling: Defects or complaints trigger comprehensive batch checks or random sampling.

• Joint Appraisal: If products fail MOHW standards within the 2-year shelf life, a joint appraisal with health authorities or 3rd-parties is initiated.

• Liability: The manufacturer is liable for compensation, replacements, and legal claims arising from production, storage, or transport defects.