Colgate-Palmolive
Hygiene products, tissues and household care products.
Colgate-Palmolive manufactures hygiene products, tissues and household care products from its New York operations. The company supplies pharmacy channels, grocery chains, institutional buyers or export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- New York, United States
- Founded
- 1806
- Website
- colgatepalmolive.com
- Categories
- Personal Care, Cleaning & Household Supplies, Medical & Healthcare Supplies
- Markets
- United States, Canada, Mexico, Brazil
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- fda-registered (green), checked 2026-08-08 FDA
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- customer-reviews (amber), checked 2026-08-08 Sitejabber
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- 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
- places-goods-on-market (green), checked 2026-08-07 US FDA National Drug Code Directory (listed drug labeler)
- 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)
- facility-registered (green), checked 2026-08-04 US EPA Facility Registry Service
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)