Replens™ Silky Smooth Personal Lubricant

GUDID 00022600001089

CHURCH & DWIGHT CO., INC.

Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant
Primary Device ID00022600001089
NIH Device Record Key052ca7d0-0a78-4fba-9a08-35cfdb8b7749
Commercial Distribution StatusIn Commercial Distribution
Brand NameReplens™ Silky Smooth Personal Lubricant
Version Model Number00022600001089
Company DUNS001211952
Company NameCHURCH & DWIGHT CO., INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com
Phone+1(800)833-9532
EmailConsumer.Relations@churchdwight.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100022600001089 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NUCLubricant, personal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-08-07
Device Publish Date2016-10-14

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80022600901255 - First Response™ Pregnancy Early Result2023-07-06 Pregnancy Kit
00022600019558 - First Response™ Pregnancy Pro Digital Pregnancy Test & App Access2023-07-06

Trademark Results [Replens]

Mark Image

Registration | Serial
Company
Trademark
Application Date
REPLENS
REPLENS
77065316 3409927 Live/Registered
CHURCH & DWIGHT CO., INC.
2006-12-15
REPLENS
REPLENS
73820226 1591663 Live/Registered
COLUMBIA LABORATORIES, INC.
1989-08-21

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