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Church & Dwight Co., Inc.

Last updated September 17, 2026

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 1 of 5

Device	Model / Reference	Registries	Class	Status
Trojan™ Premium Latex Condoms Her Pleasure™ Ecstasy™	00022600973270	FDA UDI	Class II	Active
Trojan Nirvana Collection Breathless Sample	00022600999201	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Sensitivity Pack	00022600952978	FDA UDI	Class II	Active
Trojan Willa Lubricant	00022600999379	FDA UDI	Class II	Active
Trojan™ XOXO Ultra Thin Condoms	00022600998488	FDA UDI	Class II	Active
Trojan G Condom	00022600999317	FDA UDI	Class II	Active
Trojan Ultra Thin Condom	00726893113992	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms ENZ™ Armor™	00022600932529	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms ENZ™ Latex Non-Lubricated Condoms	00022600920502	FDA UDI	Class II	Active
Trojan Pleasure Pack	00022600999560	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Ultra Ribbed Ecstasy™	00022600947400	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Ultra Thin	00022600926429	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Stimulations Intense	00022600946526	FDA UDI	Class II	Active
Trojan Raw - Non Latex	00022600999836	FDA UDI	Class II	Active
Trojan UltraFit Comfort Feel	00022600001409	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Groove™	00022600019534	FDA UDI	Class II	Active
Trojan Enz	00726893112544	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms MAGNUM™ Large Size Condoms BareSkin™	00022600228875	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms Sensitivity BareSkin™	00022600926740	FDA UDI	Class II	Active
Trojan Magnum Condom	00022600002338	FDA UDI	Class II	Active
Trojan G Condoms	00022600002000	FDA UDI	Class II	Active
Trojan Bareskin Raw	00022600001454	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Large Size Condoms Thin	00022600646143	FDA UDI	Class II	Active
Trojan™ Lubricants Tingly Warmth	00022600092667	FDA UDI	Class II	Active
Trojan All the Feels Condom	00022600300007	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms ENZ™ Lubricated Condoms	00022600900016	FDA UDI	Class II	Active
CVS Health™ Long-Lasting Feminine Moisturizer	00050428285183	FDA UDI	Class II	Active
Trojan ULTRA FIT Freedom Feel Condom	00022600001430	FDA UDI	Class II	Active
Therabreath Lozenge	00697029118832	FDA UDI	U	Active
Answer™ Pregnancy Test & Reassure	00022600998631	FDA UDI	Class II	Unknown
Trojan™ Pleasure Pack	00022600002291	FDA UDI	Class II	Active
Trojan Supra™ Premium Condoms Non-Latex Bareskin™	00022600902201	FDA UDI	Class II	Active
First Response™ Pregnancy Rapid Result Pregnancy Test Kit	00022600901266	FDA UDI	Class II	Active
Trojan XOXO Ultra Thin Mini Travel Pack	00022600016502	FDA UDI	Class II	Active
Trojan™ ENZ™ Latex Lubricated Condoms	00022600930501	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Lubricated Condoms	00022600020158	FDA UDI	Class II	Active
Trojan On the DBL	00022600000723	FDA UDI	Class II	Active
First Response™ Pregnancy Gold™ Digital Pregnancy Test	00022600901402	FDA UDI	Class II	Active
Therabreath Lozenge	00697029340103	FDA UDI	U	Active
Trojan G Condom	00022600002277	FDA UDI	Class II	Active
Therabreath Rinse	00697029507032	FDA UDI	U	Active
Trojan™ Premium Latex Condoms Ecstasy™ Pack	00022600228905	FDA UDI	Class II	Active
Trojan Ultra Thin Condom	00726893114005	FDA UDI	Class II	Active
Replens™ Long-Lasting Vaginal Moisturizer	00022600001041	FDA UDI	Class II	Active
Trojan™ Lubricants Premium Collection Tonight™	00022600000112	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms Platinum Pack	00022600953036	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasures Fire & Ice™	00022600960034	FDA UDI	Class II	Active
Trojan Enz Condom	00022600030454	FDA UDI	Class II	Active
Trojan GOAT 10ct	00022600800149	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Ultra Ribbed Value Pack	00022600949510	FDA UDI	Class II	Active

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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.

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.