| Primary Device ID | 00022600001119 |
| NIH Device Record Key | a033f64d-2047-4783-800a-3ddc229906e3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RepHresh™ Vaginal Gel Personal Lubricant |
| Version Model Number | 00022600001119 |
| Company DUNS | 001211952 |
| Company Name | CHURCH & DWIGHT CO., INC. |
| Device Count | 4 |
| 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 | 00022600001119 [Primary] |
| GS1 | 80022600001115 [Unit of Use] |
| 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 | 2016-10-14 |
| 00022600987628 | 00022600987628 |
| 00022600019657 | 00022600019657 |
| 00022600001119 | 00022600001119 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REPHRESH 90628991 not registered Live/Pending |
Restore RX Beauty LLC 2021-04-07 |
![]() REPHRESH 87710628 not registered Live/Pending |
CHURCH & DWIGHT CO., INC. 2017-12-06 |
![]() REPHRESH 79316315 not registered Live/Pending |
LIN Xijian 2021-04-20 |
![]() REPHRESH 78912034 not registered Dead/Abandoned |
Hikari Holdings, L.C. 2006-06-20 |
![]() REPHRESH 77065321 3591790 Live/Registered |
CHURCH & DWIGHT CO., INC. 2006-12-15 |
![]() REPHRESH 76317240 2757069 Live/Registered |
CHURCH & DWIGHT CO., INC. 2001-09-26 |