Replens Long-Lasting Vaginal Moisturizer

GUDID 00022600987611

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 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 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 ID00022600987611
NIH Device Record Key8d687e3a-f16b-42f2-acc0-41a0a482e138
Commercial Distribution StatusIn Commercial Distribution
Brand NameReplens Long-Lasting Vaginal Moisturizer
Version Model Number00022600987611
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-Countertrue

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
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
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
GS100022600987611 [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 Number4
Public Version Date2020-08-07
Device Publish Date2018-02-27

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