PZ Cussons Nigeria
Soaps, detergents, personal-care products and household goods.
PZ Cussons Nigeria manufactures soaps, detergents, personal-care products and household goods from its Lagos operations. The company supplies pharmacy channels, grocery chains, institutional buyers or export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- Lagos, Nigeria
- Founded
- 1899
- Website
- pzcussons.com.ng
- Categories
- Personal Care, Cleaning & Household Supplies, Medical & Healthcare Supplies
- Markets
- Nigeria, Ghana, Kenya, South Africa
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- workforce-on-record (green), checked 2023-12-31 National Pension Commission of Nigeria, schedule of employers issued with compliance certificates
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
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)