Primary Device ID | 00022600001072 |
NIH Device Record Key | 4228b849-0bfa-448c-b95c-7dadfa5f26b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Replens™ Long-Lasting Vaginal Moisturizer |
Version Model Number | 00022600001072 |
Company DUNS | 001211952 |
Company Name | CHURCH & DWIGHT CO., INC. |
Device Count | 1 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00022600001072 [Primary] |
NUC | Lubricant, personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-08-07 |
Device Publish Date | 2017-03-31 |
00022600001072 | 00022600001072 |
00022600001041 | 00022600001041 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
REPLENS 77065316 3409927 Live/Registered |
CHURCH & DWIGHT CO., INC. 2006-12-15 |
REPLENS 73820226 1591663 Live/Registered |
COLUMBIA LABORATORIES, INC. 1989-08-21 |