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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 5 of 5

Device	Model / Reference	Registries	Class	Status
Therabreath Lozenge	00697029774694	FDA UDI	U	Active
Trojan™ The Edge Changing Sensations Condom	00022600001324	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Her Pleasure™ Sensations	00022600973201	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Double Ecstasy™	00022600906681	FDA UDI	Class II	Active
Trojan™ The Edge Changing Sensations Condom	00022600016519	FDA UDI	Class II	Active
Trojan Ultra Thin w/ Spermicide	00022600002369	FDA UDI	Class II	Active
Trojan BareSkin RAW	00022600200024	FDA UDI	Class II	Active
Pre-Seed™ Personal Lubricant Fertility Friendly Pre-filled Applicators	00055114999061	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms ENZ™ Armor Spermicidal Lubricant	00022600931508	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasure Pack	00022600953210	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Sensitivity Ultra Thin Travel Pack	00022600998969	FDA UDI	Class II	Active
Trojan Variety Pack	00022600999492	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms MAGNUM™ Large Size Condoms BareSkin™	00022600228882	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Fire & Ice™	00022600960126	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pure Ecstasy™	00022600998563	FDA UDI	Class II	Active
Trojan Xoxo Ultra Thin 24ct	00022600019824	FDA UDI	Class II	Unknown
Trojan Discovery Pack	00022600029274	FDA UDI	Class II	Active
Pre-Seed™ Fertility Lubricant	K193450	FDA 510(k)	Class II	Active
Trojan Magnum Condom With Fire & Ice Lubricant	K120287	FDA 510(k)	Class II	Active
Trojan XOXO Thin Male Natural Rubber Latex Condom with Silicone and Aloe Lubricant	K161545	FDA 510(k)	Class II	Active
Trojan Riviera Personal Lubricant	K150886	FDA 510(k)	Class II	Active
Trojan Supra Lubricated Polyurethane Male Condom	K100767	FDA 510(k)	Class II	Active
Nirvana B Personal Lubricant	K120751	FDA 510(k)	Class II	Active
Nirvana D Personal Lubricant (tbd)	K123427	FDA 510(k)	Class II	Active
TrojanTM Azul Personal Lubricant (H2O Sensitive Touch Personal Lubricant)	K180764	FDA 510(k)	Class II	Active
Trojan Her Pleasure (ribbed) Ecstasy Latex Condom With Lubricant	K120286	FDA 510(k)	Class II	Active
TROJAN Fire & Ice lubricated male natural rubber latex condom	K221906	FDA 510(k)	Class II	Active
TROJAN SIS Synthetic Latex Condom with Silicone Lubricant	K240379	FDA 510(k)	Class II	Active
Trojan Thintensity Brand Male Latex Condom Lubricated With Ultrasmooth And Warm Sensations Lubricant	K073016	FDA 510(k)	Class II	Active
Trojan Thintensity Brand Male Latex Condom	K071272	FDA 510(k)	Class II	Active
Trojan-Enz Brand	K071313	FDA 510(k)	Class II	Active
Azul Personal Lubricant	K141034	FDA 510(k)	Class II	Active
Trojan Supra Lubricated Polyurethane Male Condom	K050828	FDA 510(k)	Class II	Active
Trojan Chain Reaction Personal Lubricant	K161544	FDA 510(k)	Class II	Active
Trojan Jaguar Male Natural Rubber Latex Condom With Warming And Tingling Lubricant	K131887	FDA 510(k)	Class II	Active
First Response Early Result Pregnancy Test (otc)	K083716	FDA 510(k)	Class II	Active
First Response Gold Digital Pregnancy Test	K070054	FDA 510(k)	Class II	Active
Nirvana A Personal Lubricant	K120706	FDA 510(k)	Class II	Active
Trojan Chain Reaction Natural Rubber Latex Condom with Sensate Lubricant	K180104	FDA 510(k)	Class II	Active
First Response Early Result Pregnancy Test	K123436	FDA 510(k)	Class II	Active
Trojan Supra Lubricated Polyurethane Male Condom	K171639	FDA 510(k)	Class II	Active
TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant	K221431	FDA 510(k)	Class II	Active
First Response Gold Digital Pregnancy Test	K123567	FDA 510(k)	Class II	Active
Replens Long-Lasting Vaginal Moisturizer	K203818	FDA 510(k)	Class II	Active
Trojan™ Ultra Ribbed Ecstasy latex condom with lubricant (Trojan™ Ultra Ribbed Ecstasy)	K243640	FDA 510(k)	Class II	Active
Trojan XOXO Ribbed Male Natural Rubber Latex Condom with Silicone and Aloe Lubricant	K161915	FDA 510(k)	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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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.