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Church & Dwight Co., Inc.

Last updated September 17, 2026

What Church & Dwight Co., Inc. makes

Church & Dwight Co., Inc. manufactures sexual health products including male condoms made from latex, synthetic polymers, and animal-derived materials, as well as sexual lubricants and artificial saliva.

The company's products are regulated as Class I and Class II medical devices in the US and are listed in the FDA 510(k) and FDA UDI registries. Church & Dwight Co., Inc. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What products does Church & Dwight Co., Inc. manufacture?

Where is Church & Dwight Co., Inc. based?

Church & Dwight Co., Inc. is based in the United States.

Which regulatory registries list Church & Dwight Co., Inc.'s devices?

Church & Dwight Co., Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries.

How are Church & Dwight Co., Inc.'s devices classified?

Church & Dwight Co., Inc.'s devices are regulated as Class I and Class II medical devices in the US, with some devices also classified as U (unclassified).

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: 469 NORTH HARRISON STREET, PRINCETON, NJ, 08543
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2280705
DUNS Number: —

Catalogue (246)

Page 2 of 5

Device	Model / Reference	Registries	Class	Status
Answer™ Pregnancy Test	00022600408123	FDA UDI	Class II	Unknown
Trojan 100ct Bulk Mix	00022600019831	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Sensitivity Ultra Thin Armor™	00022600927426	FDA UDI	Class II	Active
Replens™ Long-Lasting Vaginal Moisturizer	00022600001072	FDA UDI	Class II	Active
Trojan ENZ Lubricated Condoms	00022600937098	FDA UDI	Class II	Active
Trojan The Edge	00022600000983	FDA UDI	Class II	Active
Trojan Enz	00726893114104	FDA UDI	Class II	Active
Trojan Magnum Lubricated Condoms	00022600642091	FDA UDI	Class II	Active
Trojan Ultra Ribbed Condom	00726893800021	FDA UDI	Class II	Active
Replens Long-Lasting Vaginal Moisturizer	00022600987611	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Nirvana	00022600020196	FDA UDI	Class II	Active
Trojan HotSpot Vibrating Ring and 1 Ultra Thin Condom	00022600906674	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Ultra Ribbed	00022600000617	FDA UDI	Class II	Active
Trojan Magnum XL Condom	00022600002345	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Double Ecstasy™	00022600019619	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms MAGNUM™ Large Size Condoms BareSkin™	00022600019763	FDA UDI	Class II	Active
TROJAN™ NaturaLamb™ Luxury Condoms	00022600987536	FDA UDI	Class II	Active
Trojan Magnum Lubricated Condom	00726893112605	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Sensitivity Ultra Thin	00022600926207	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms ENZ™ Value Pack	00022600939511	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms XL	00022600647140	FDA UDI	Class II	Active
Therabreath Lozenge	00697029724729	FDA UDI	U	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms	00022600642039	FDA UDI	Class II	Active
RepHresh™ Clean Balance™ Feminine Freshness 2-Step Kit	00022600001133	FDA UDI	Class II	Unknown
Trojan™ Gel Lubricants Explore™ Just Pure Fun™	00022600000013	FDA UDI	Class II	Unknown
Trojan™ Premium Latex Condoms Ultra Ribbed Ecstasy™	00022600947219	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Ecstasy™	00022600647201	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms Studded BareSkin™	00022600228899	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Ultra Ribbed	00022600947523	FDA UDI	Class II	Active
Trojan Enz	00726893112537	FDA UDI	Class II	Active
First Response™ Pregnancy Test & Confirm Pregnancy	00022600901334	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms ENZ™ Non-Lubricated	00022600907527	FDA UDI	Class II	Active
Pre-Seed™ Personal Lubricant Fertility Friendly	00855114000961	FDA UDI	Class II	Active
Trojan Magnum	00726893114043	FDA UDI	Class II	Active
Trojan Ultra Thin Condoms	00726893113985	FDA UDI	Class II	Active
Trojan Bareskin Raw	00022600001539	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Sensitivity Ultra Thin Armor™	00022600927204	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Nirvana	00022600020387	FDA UDI	Class II	Active
Trojan Premium Latex Condoms Utlra Ribbed	00022600019459	FDA UDI	Class II	Active
Trojan Ultra Ribbed Condom	00726893112575	FDA UDI	Class II	Active
First Response™ Pregnancy Early Result	00022600001317	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Stimulations Twisted™	00022600976523	FDA UDI	Class II	Active
Simply Saline® Contact Lenses Sterile Saline Solution	00022600017172	FDA UDI	Class II	Active
Trojan GOAT 3ct	00022600800132	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Her Pleasure™ Sensations	00022600937524	FDA UDI	Class II	Active
Trojan Bareskin Raw	00022600001553	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Nirvana	00022600999218	FDA UDI	Class II	Active
Therabreath Lozenge	00697029471005	FDA UDI	U	Active
Trojan™ Premium Latex Condoms Magnum™ Lubricated Condoms	00022600019442	FDA UDI	Class II	Active
Trojan UltraFit Sensitive Tip Feel	00022600001416	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (12)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Church & Dwight Co., Inc. has 12 recall records, with the earliest initiated on 2011-12-22 and the most recent on 2023-01-25. The recorded statuses include open, classified, and terminated. Reasons for recalls include marketing First Response Pregnancy Kits with an app without a new 510k, potential app misreading of test results, contamination of Sodium Bicarbonate, and addressing a choking hazard with Spinbrush brush heads beyond the recommended 3-month life.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jan 25, 2023	Z-1350-2023	—	open, classified	Church & Dwight First Response Pregnancy Kits was marketed with the Easy Read App without a new 510k. There is also a potential for Easy Read App to be unable to reads the test results (i.e., no results reported on the APP screen) or to misread the analog results shown on the pregnancy test stick and may lead to misinterpretation of false positive or false negative tests by the user.
Jun 11, 2013	Z-1811-2013	—	terminated	Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate, USP produced by the Old Fort, OH Sodium Bicarbonate Production facility due to metal and other contamination.
Dec 22, 2011	Z-2094-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-2093-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-0857-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-2096-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-2099-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-2097-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-0858-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-2095-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-2098-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Dec 22, 2011	Z-0859-2012	—	terminated	Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.