Is this your brand? Sign in to claim ownership.

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 4 of 5

Device	Model / Reference	Registries	Class	Status
Trojan™ Premium Latex Condoms ENZ™ Armor™ Value Pack	00022600933519	FDA UDI	Class II	Active
Well at Walgreens Long-Lasting Feminine Moisturizer & Lubricating Gel	00311917184616	FDA UDI	Class II	Active
First Response™ Pregnancy Pro Digital Pregnancy Test & App Access	00022600019558	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Stimulations Ultra Ribbed	00022600940500	FDA UDI	Class II	Active
Trojan Ultra Ribbed Condom	00022600999386	FDA UDI	Class II	Active
Trojan Her Pleasure Condom	00022600999409	FDA UDI	Class II	Active
Trojan UltraFit Bare Feel	00022600001423	FDA UDI	Class II	Active
Trojan Ultra Ribbed	00726893112599	FDA UDI	Class II	Active
Trojan Ultra Thin Condom	00726893800014	FDA UDI	Class II	Active
Trojan™ Gel Lubricants Explore™ Just Pure Fun™	00022600000020	FDA UDI	Class II	Unknown
Trojan Willa Ribbed Condom	00022600500001	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Intensified Charged™	00022600957010	FDA UDI	Class II	Active
First Response Early Result Pregnancy Test	00022600020141	FDA UDI	Class II	Active
Trojan Magnum Gold Collection	00022600019879	FDA UDI	Class II	Active
Trojan Lubricant Chain Reaction Sample 2ml	00022600998471	FDA UDI	Class II	Active
Therabreath Lozenge	00697029241127	FDA UDI	U	Active
Trojan™ Premium Latex Condoms Ultra Ribbed Ecstasy™	00022600947325	FDA UDI	Class II	Active
Trojan™ Lubricants Water-Based H2O Sensitive Touch	00022600000068	FDA UDI	Class II	Active
Trojan™ Lubricants Continuous Silkiness	00022600092650	FDA UDI	Class II	Unknown
TROJAN™ NaturaLamb™ Luxury Condoms	00022600998440	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasures Extended	00022600972525	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Her Pleasure™ Sensations Armor™	00022600974529	FDA UDI	Class II	Active
First Response™ Pregnancy Rapid Result Pregnancy Test	00022600649168	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Sensitivity Thintensity	00022600926733	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasures Extended	00022600019961	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Pleasure Pack	00022600020165	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Magnum™ Fire & Ice™	00022600649151	FDA UDI	Class II	Active
Trojan Bareskin Raw	00022600002901	FDA UDI	Class II	Active
Trojan Ecstasy Ultra Ribbed Lubricated Condom	00022600900238	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms BareSkin™ Value Pack	00022600998532	FDA UDI	Class II	Active
Trojan Variety Pack BareSkin	00022600001546	FDA UDI	Class II	Active
Trojan All The Feels Variety Pack	00022600000709	FDA UDI	Class II	Active
RepHresh™ Vaginal Gel Personal Lubricant	00022600001119	FDA UDI	Class II	Unknown
RepHresh™ Vaginal Gel Personal Lubricant	00022600019657	FDA UDI	Class II	Active
TROJAN™ Premium Latex Condoms Platinum Pack	00022600998525	FDA UDI	Class II	Active
Trojan™ Lubricants Premium Collection Riviera™	00022600000303	FDA UDI	Class II	Active
Trojan Magnum Lubricated Condom	00726893112612	FDA UDI	Class II	Active
Trojan Magnum Condom	00726893114098	FDA UDI	Class II	Active
Trojan™ Sensitivity Pack	00022600001492	FDA UDI	Class II	Active
First Response™ Pregnancy Triple Check Pregnancy Test Kit	00061700900700	FDA UDI	Class II	Active
First Response™ Pregnancy Early Result Pregnancy Test	00022600901259	FDA UDI	Class II	Active
Trojan™ Premium Latex Condoms Fire & Ice™ Ecstasy™	00022600975205	FDA UDI	Class II	Active
Trojan Magnum Raw	00022600200161	FDA UDI	Class II	Active
RepHresh™ Vaginal Gel Personal Lubricant	00022600987628	FDA UDI	Class II	Unknown
Trojan™ Premium Latex Condoms Pleasure Pack	00022600019466	FDA UDI	Class II	Active
Trojan Ultra Thin Armor	00022600999539	FDA UDI	Class II	Active
Therabreath Rinse	00697029383414	FDA UDI	U	Active
Trojan Magnum Raw	00022600200147	FDA UDI	Class II	Active
Trojan™ Ultra Thin Bulk	00022600000310	FDA UDI	Class II	Active
Troj Bareskin Raw 500	00022600221500	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.