| Primary Device ID | 00022600987611 |
| NIH Device Record Key | 8d687e3a-f16b-42f2-acc0-41a0a482e138 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Replens Long-Lasting Vaginal Moisturizer |
| Version Model Number | 00022600987611 |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00022600987611 [Primary] |
| NUC | Lubricant, personal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-08-07 |
| Device Publish Date | 2018-02-27 |
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| 80022600901255 - First Response™ Pregnancy Early Result | 2023-07-06 Pregnancy Kit |
| 00022600019558 - First Response™ Pregnancy Pro Digital Pregnancy Test & App Access | 2023-07-06 |