TROJAN XOXO ULTRA THIN 24CT

GUDID 00022600019824

CHURCH & DWIGHT CO., INC.

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• Primary Device ID: 00022600019824
• NIH Device Record Key: 24f757fd-aedb-4560-a50f-47018ec377fa
• Commercial Distribution Discontinuation: 2021-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: TROJAN XOXO ULTRA THIN 24CT
• Version Model Number: 00022600019824
• Company DUNS: 001211952
• Company Name: CHURCH & DWIGHT CO., INC.
• Device Count: 24
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00022600019824 [Primary]
GS1	80022600998491 [Unit of Use]

FDA Product Code

• HIS: CONDOM

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-09-29
• Device Publish Date: 2017-02-02

Devices Manufactured by CHURCH & DWIGHT CO., INC.

• 00022600019824 - TROJAN XOXO ULTRA THIN 24CT: 2023-09-29
• 00022600019824 - TROJAN XOXO ULTRA THIN 24CT: 2023-09-29
• 00022600998495 - TROJAN CONDOM XOXO ULTRA THIN 10CT: 2023-09-29
• 00022600902201 - Trojan Supra™ Premium Condoms Non-Latex Bareskin™: 2023-09-27 For Contraception Plus STI Protection
• 00022600902423 - Trojan Supra™ Premium Condoms Non-Latex Bareskin™: 2023-09-27 For Contraception Plus STI Protection
• 00022600019466 - Trojan™ Premium Latex Condoms Pleasure Pack: 2023-09-21 Pack contains Trojan Double Ecstasy Trojan Charged Trojan Ultra Ribbed Trojan ENZ
• 00022600020165 - Trojan™ Premium Latex Condoms Pleasure Pack: 2023-09-21 Pack contains: Trojan Double Ecstasy Trojan Ultra Thin Trojan Fire & Ice Trojan Ultra Ribbed Trojan ENZ
• 80022600901255 - First Response™ Pregnancy Early Result: 2023-07-06 Pregnancy Kit
• 00022600019558 - First Response™ Pregnancy Pro Digital Pregnancy Test & App Access: 2023-07-06