Reckitt Benckiser
Global manufacturer of hygiene, health, and nutrition brands including Dettol, Lysol, and Durex.
Reckitt is a British multinational producing market-leading hygiene and health consumer goods across over 60 countries. Its wholesale B2B catalogue includes household disinfectants, sexual health products, infant nutrition, and OTC health products sold through retailers, hospitals, and institutional buyers globally. Manufacturing is concentrated in the UK, Germany, India, and the US, with robust quality systems across all sites. Trade partners access products via Reckitt's regional commercial teams, approved distributors, and B2B purchasing platforms. The company's brands consistently hold top-two market positions in their categories.
- Type
- Manufacturer
- Location
- Slough, United Kingdom
- Founded
- 1900
- Website
- reckitt.com
- Categories
- Cleaning & Household Supplies, Medical & Healthcare Supplies, Personal Care
- Markets
- United Kingdom, United States, Germany, India, China, Brazil, Australia, France, South Africa, Mexico
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- directors-on-file (green), checked 2026-06-20 Companies House
- registered-since (green), checked 1953-12-23 Companies House free company data product (UK)
- ch-active (green), checked 2026-06-20 Companies House
- media-mention (green), checked 2026-07-18 TradingView
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 22000, Food Safety IAF CertSearch
- Good Manufacturing Practice
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)