Dr's Formula Antibacterial Hand Wash contains the antibacterial agent "Chlorhexidine Digluconate", which mainly destroys the permeability barrier on the bacterial cytoplasmic membrane. In addition to inhibiting bacteria, it can also kill general bacteria. The product has been verified by a third-party impartial unit (Hwayo Tech & Lab. LTD.) and is effective against the five major bacteria, including Escherichia coli, Pseudomonas aeruginosa, Salmonella, Staphylococcus aureus, and Fecal Streptococcus, with an antibacterial rate of up to 99.9% . Refreshing and clean formula, fast foaming power and strong moisturizing properties. The foam is fine, gentle and non-irritating, and can quickly penetrate into the gaps between nails and cuticles to effectively remove dirt. The natural skin care ingredient "lanolin" replenishes the oil lost due to hand washing. It has an elegant and refreshing fragrance and is effective in removing fishy odor. This gentle product not only can thoroughly wash away dirt, but also can relieve the dryness and discomfort caused by hand washing, and also has the effect of cleaning and softening hands.
Formosa Biomedical Technology Corporation has long emphasized product quality and consumer safety and has established internationally recognized quality management systems. The company has obtained GMP (Good Manufacturing Practice) certification and ISO 22716 Cosmetics GMP international certification, demonstrating compliance with global standards in cosmetic manufacturing, quality management, and production processes.
To ensure stable product quality, the company strictly follows Cosmetic GMP across all processes, including raw materials, production, equipment maintenance, hygiene, training, quality inspection, and document control. Since obtaining GMP certification in November 2007, it has undergone re-certification audits every three years to ensure compliance and continuous improvement.
ISO 22716 is an international cosmetic GMP guideline issued by ISO. It emphasizes GMP principles, risk management, hygiene control, documentation traceability, and process control. Through SOPs and batch traceability, companies manage the full product lifecycle from raw materials to final release, improving quality and competitiveness.
In the future, Formosa Biomedical Technology Corporation will continue to follow GMP and ISO 22716 international standards, enhance its quality management systems and manufacturing technologies, and provide consumers with safer, more reliable, and higher-quality products, fulfilling its commitment to product quality and consumer health.
Aqua, Sodium Laureth Sulfate, Lauric Acid, Sodium Chloride, Cocamidopropyl Betaine, Cocamide MEA, Potassium Hydroxide, Glycol Distearate, Fragrance, Phenoxyethanol, Glycerin, PEG-75 Lanolin, Disodium EDTA, Chlorhexidine Digluconate, o-Cymen-5-ol
Chlorhexidine Digluconate
Formosa Biomedical Technology Corp.
Raw materials: The quality control unit inspects all purchased raw materials according to established specifications and supplier Certificate of Analysis (COA), as recorded in the material inspection form. External testing may be commissioned when necessary to ensure compliance. Only materials meeting acceptance standards are released and marked as “Qualified Release.” The supplier COA is used as reference for storage conditions and quality standards.
Semi-finished products: Each batch is assigned a production batch number for identification and traceability to finished goods. The quality control team performs in-process random inspections according to defined procedures and acceptance criteria. If results fail to meet standards, an investigation and deviation report are issued to the manufacturing unit for corrective action. Semi-finished products are stored under appropriate environmental conditions, in designated areas and containers, with defined maximum storage periods.
Finished products: All finished products undergo final quality control inspection before release. Results are recorded in the “Quality Inspection Record Form.” Only products passing all requirements are approved for release and distribution. Finished products are stored under suitable environmental conditions according to product characteristics and are clearly separated from non-conforming products to prevent mix-ups.
Dr’s Formula Antibacterial Hand Wash has passed safety testing conducted by a third-party professional laboratory. Test items included formaldehyde and six heavy metals (lead, mercury, arsenic, cadmium, antimony, and nickel). The results complied with relevant regulations and quality standards, confirming the product is safe for use.
Raw Materials: Cosmetic raw materials are purchased from qualified suppliers according to established specifications and acceptance standards. Suppliers may be evaluated through questionnaires or audits. Upon receipt, warehouse personnel verify shipping documents and packaging integrity. Materials with defects that may affect quality are isolated and clearly identified until disposition is determined. Labels include product name, supplier name, receipt date, and batch information.
Semi-Finished Products: Documented procedures are established for each manufacturing stage. Authorized batch records are issued before production. Manufacturing follows approved formulas, batch numbers, and operating procedures. Each batch is assigned a unique batch number for traceability. QC performs in-process inspections according to acceptance criteria. Nonconforming results are investigated and corrective actions are required. Semi-finished products are stored under suitable conditions in designated areas with defined storage periods.
Finished Products: Finished products must comply with QC quality standards. Before release, all products undergo QC inspection and results are documented. Only qualified products may be released. Finished products are stored under appropriate conditions and separated from nonconforming products. Returned products are clearly identified, stored in designated areas, and evaluated by QC for proper disposition.
