Suppliers / Church & Dwight

Church & Dwight

United States Updated 9 July 2026

Church & Dwight is a finished-dose manufacturer based in United States. It appears in 72 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, MHRA (UK) and EDE (AE). Its GMP standing is certified by US FDA and NAFDAC (NG). Its most recent recorded inspection, by US FDA, closed on 7 February 2025 as VAI.

0
active US DMFs
0
valid CEPs
6
registered plants 4 with an FDA FEI number
72
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
4 of 4 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 7 February 2025 VAI US FDA
  • 25 October 2024 VAI US FDA
  • 22 August 2024 NAI US FDA
  • 12 July 2023 VAI US FDA
  • 17 January 2020 VAI US FDA
  • 23 May 2019 VAI US FDA
  • 27 April 2018 VAI US FDA
  • 8 December 2017 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
QC, United Arab Emirates Not on file
Folkestone, United Arab Emirates Not on file
Canada, Canada 1000657351
Lakewood, United States 2224549
Old Fort, United States 1525647
Green River, United States 1713902

What they file, and where

Molecule Regulators Docs
Sodium Bicarbonate SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Benzocaine finished dose Bisacodyl finished dose Capsaicin finished dose Dimenhydrinate finished dose Levomenthol finished dose Simethicone finished dose

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 23 None
MHRA (UK) 11 None
EDE (AE) 11 None
DIGEMAPS (DO) 11 None
MINSA (CR) 9 None
EMA 6 None
US FDA None 4
NAFDAC (NG) None 1

Questions about Church & Dwight

Does Church & Dwight hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Church & Dwight. It does have 72 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Church & Dwight FDA-registered?
4 sites operated by Church & Dwight carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Church & Dwight's last inspection go?
The most recent inspection on record closed on 7 February 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file.
Where does Church & Dwight manufacture?
6 registered sites are on record, in United Arab Emirates, Canada and United States (QC, Folkestone and Canada among others). Every site is listed on this page with the register it came from.
What does Church & Dwight make?
1 molecule is on record against Church & Dwight, including Sodium Bicarbonate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Church & Dwight's GMP?
Current GMP certificates are on record from US FDA and NAFDAC (NG). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 7 February 2025.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates