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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 3 of 5

Device	Model / Reference	Registries	Class	Status
Trojan™ Lubricants Premium Collection Arouses & Releases™*	00022600959632	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Her Pleasure™ Sensations	00022600973522	FDA UDI	Class II	Active
Troj Variety Pack BareSkin	00022600001577	FDA UDI	Class II	Active
First Response™ Pregnancy Comfort Sure Design Early Result Pregnancy Test	00022600901273	FDA UDI	Class II	Active
Simply Saline™ Sterile Saline Solution Wound Wash	00022600085522	FDA UDI	U	Active
Trojan Supra™ Premium Condoms Non-Latex Bareskin™	00022600902423	FDA UDI	Class II	Active
Trojan Ultra Ribbed Condom	00726893112582	FDA UDI	Class II	Active
Trojan Pleasure Pack Condoms	00022600002352	FDA UDI	Class II	Active
Trojan™ Ultra Thin Sample	00022600999263	FDA UDI	Class II	Active
TROJAN™ NaturaLamb™ Luxury Condoms	00022600980506	FDA UDI	Class II	Active
First Response™ Ovulation Daily Digital Ovulation Test	00022600408000	FDA UDI	Class I	Active
Trojan Thintensity Condom	00726893113466	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum Large Size Condoms Value Pack	00022600642374	FDA UDI	Class II	Active
First Response Early Result Pregnancy Test	00022600978633	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasure Pack	00022600953388	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Double Ecstasy™ Value Pack	00022600019626	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms Sensitivity BareSkin™	00022600957058	FDA UDI	Class II	Active
Trojan Willa Thin Condom	00022600500018	FDA UDI	Class II	Active
Trojan G Condom	00022600002284	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasure Pack	00022600953029	FDA UDI	Class II	Active
Trojan Pleasure Pack	00022600030461	FDA UDI	Class II	Active
Trojan Variety Pack BareSkin	00022600999652	FDA UDI	Class II	Active
Trojan Discovery Pack	00022600029267	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Gold Pack	00022600643203	FDA UDI	Class II	Active
First Response™ Pregnancy Triple Check Pregnancy Test Kit	00022600020202	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Stimulations Ultra Ribbed Armor™	00022600945529	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Thin	00022600646037	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Charged™	00022600957003	FDA UDI	Class II	Active
Trojan Enz Lubricated Latex Condom	00726893112551	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms BareSkin™ Lubricated Condoms	00022600019435	FDA UDI	Class II	Active
Trojan Lubricant Chain Reaction 2.7oz	00022600998464	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms	00022600642145	FDA UDI	Class II	Active
Replens™ Silky Smooth Personal Lubricant	00022600001089	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Ecstasy™	00022600643135	FDA UDI	Class II	Active
Answer™ Ovulation Test Daily Tracker	00022600407089	FDA UDI	Class I	Active
Trojan™ Premium Latex Condoms Sensitivity Ultra Thin Value Pack	00022600926610	FDA UDI	Class II	Active
First Response Comfort Check Pregnancy Test Kit	00022600999645	FDA UDI	Class II	Active
Trojan™ Lubricants Water-Based H2O Closer™	00022600000051	FDA UDI	Class II	Active
Simply Saline™ Sterile Saline Solution Wound Wash	00022600085539	FDA UDI	U	Active
Pre-Seed™ Personal Lubricant Fertility Friendly	00855114000992	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum Large Size Condoms Ribbed	00022600642084	FDA UDI	Class II	Active
Trojan™ Lubricants Arouses* & Intensifies	00022600092636	FDA UDI	Class II	Active
Trojan Mangum Condom	00726893800038	FDA UDI	Class II	Active
Trojan All The Feels Variety Pack	00022600000600	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Ribbed	00022600642152	FDA UDI	Class II	Active
First Response™ Ovulation Test	00022600900542	FDA UDI	Class I	Active
Trojan Condom Xoxo Ultra Thin 10ct	00022600998495	FDA UDI	Class II	Unknown
Trojan Magnum Personal Lubricant	00022600000204	FDA UDI	Class II	Active
Trojan Ultra Ribbed Condom	00022600999485	FDA UDI	Class II	Active
Trojan Extended Pleasure Condom	00022600999393	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.