KOREA-BASED MANUFACTURER

Quasi-Drug, Oral Care
& Hygiene Product Manufacturer

S-ONE Pharmaceutical develops and manufactures oral care, hygiene and quasi-drug products in Korea. We operate in-house R&D, manufacturing facilities, quality control and product-specific documentation review.

COMPANY OVERVIEW

Manufacturing experience
built through own-brand products

S-ONE Pharmaceutical was established based on long-term manufacturing experience and has developed its manufacturing foundation through own-brand product development and supply.

We focus on oral care and hygiene product categories, with production review based on product type, formulation, packaging specification and expected quantity.

SINCE 2016

S-ONE Pharmaceutical

Established as a quasi-drug and hygiene product manufacturing company.

R&D

In-House Lab

Product development, formulation research and verification data management.

FACILITY

Factory 1 & 2

Manufacturing, office and production management facilities in Pocheon, Korea.

PRODUCT

Oral & Hygiene

Focused on oral care, hygiene, disinfectant and related product categories.

INTEGRATED MANUFACTURING PLATFORM

R&D, Manufacturing,
Quality & Documentation

S-ONE Pharmaceutical operates an integrated manufacturing system connecting in-house R&D, manufacturing facilities, quality control and product-specific documentation review.

01

R&D Center

Product development, formulation research and product-specific verification materials are managed through our in-house R&D system.

02

Manufacturing Facility

Mixing, filling and packaging facilities support production lines according to product formulation and packaging specifications.

03

Quality Control

Quality checks are managed across key stages from raw material receipt to finished product shipment.

04

Documentation

Product-related documents such as test reports, certification materials and regulatory records are reviewed by product type.

MANUFACTURING FACILITY

Facility Images

Our manufacturing facilities support mixing, filling, packaging and related production processes for oral care and hygiene product categories.

MANUFACTURING SCOPE

Product Categories We Handle

We focus on oral care, hygiene and related product categories. Production feasibility is reviewed based on formulation, packaging specification and expected quantity.

01

Oral Care Products

Toothpaste, whitening toothpaste, mouth spray, mouthwash and other oral care product categories.

02

Hygiene Products

Hand sanitizers, external-use disinfectants, hygiene sprays and daily hygiene product categories.

03

Formulation & Packaging

Liquid, gel, cream, paste and powder-type formulations with tube, pouch, pump and spray packaging review.

04

Own Brand & OEM/ODM

Based on own-brand manufacturing experience, OEM/ODM product development and production inquiries are reviewed by product specification.

QUALITY & DOCUMENTATION

Product-Specific
Quality Review

Quality and document requirements may vary by product type, formulation, packaging and market requirements.

  • Raw Material & Packaging Review Raw materials, containers, tubes, pouches, labels and cartons are reviewed according to product specification.
  • In-Process & Finished Product Check Key points such as filling condition, packaging status, labeling and finished product condition are checked by production stage.
  • Testing & Verification Materials Product-related test reports, in-house R&D data and certification materials are reviewed when required.
  • Regulatory & Export Documents Required documents may differ depending on product category, destination country and transaction purpose.
BUSINESS INQUIRY

Information Needed
for Production Review

Sharing product details and reference materials helps us review production feasibility more accurately.

  • Product Type Product category, intended use and reference product if available.
  • Reference Sample A similar finished product sample is helpful for reviewing formulation, container, texture and packaging direction.
  • Formulation & Packaging Formulation type, container, capacity, packaging material and labeling requirements.
  • Expected Quantity & Schedule Estimated order quantity and target production schedule.
  • Documents & Market Requirements Requested documents, target country and purpose of submission if export or certification materials are needed.

Contact S-ONE Pharmaceutical

For product supply, product development or OEM/ODM manufacturing inquiries, please contact us with product details, reference samples, expected quantity, packaging specifications and target schedule.

Tel +82-31-534-0037

E-mail s-one0@naver.com

Address 1073 / 1077, Jeonyeong-ro, Changsu-myeon, Pocheon-si, Gyeonggi-do, Republic of Korea