Church & Dwight
Hygiene products, tissues and household care products.
Church & Dwight manufactures hygiene products, tissues and household care products from its Ewing operations. The company supplies pharmacy channels, grocery chains, institutional buyers or export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- Ewing, United States
- Founded
- 1846
- Website
- churchdwight.com
- Categories
- Personal Care, Cleaning & Household Supplies, Medical & Healthcare Supplies
- Markets
- United States, Canada, Mexico, United Kingdom
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- fda-registered (green), checked 2026-08-08 FDA
- customer-reviews (amber), checked 2026-08-08 Sitejabber
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- registered-manufacturer (green), checked 2026-08-18 Chemistry, Food and Drugs Division, Ministry of Health of Trinidad and Tobago, register of drugs (Food and Drugs Act Chap. 30:01)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- FDA Registered FDA Establishment Registration
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)