Cleanoz is a Nasal; Ophthalmic Solution in the Human Otc Drug category. It is labeled and distributed by Laboratoires Gifrer Barbezat. The primary component is Sodium Chloride.
| Product ID | 44929-002_7336682d-094c-4f71-9e15-6854ed73e304 |
| NDC | 44929-002 |
| Product Type | Human Otc Drug |
| Proprietary Name | Cleanoz |
| Generic Name | Sodium Chloride |
| Dosage Form | Solution |
| Route of Administration | NASAL; OPHTHALMIC |
| Marketing Start Date | 2008-11-25 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part341 |
| Labeler Name | Laboratoires Gifrer Barbezat |
| Substance Name | SODIUM CHLORIDE |
| Active Ingredient Strength | 900 mg/100mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2008-11-25 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-11-25 |
| Ingredient | Strength |
|---|---|
| SODIUM CHLORIDE | 900 mg/100mL |
| SPL SET ID: | 835dc7e4-6efb-4890-af4e-eaf9469601cf |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 44929-002 | Cleanoz | Cleanoz |
| 0220-0432 | Aqua marina | SODIUM CHLORIDE |
| 0220-3582 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3583 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3586 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3587 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3590 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3593 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3595 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3596 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3597 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3598 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3599 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3600 | Natrum muriaticum | SODIUM CHLORIDE |
| 0220-3601 | Natrum muriaticum | SODIUM CHLORIDE |
| 0019-1188 | SODIUM CHLORIDE | sodium chloride |
| 0264-1800 | Sodium Chloride | Sodium Chloride |
| 0264-2201 | Sodium Chloride | Sodium Chloride |
| 0264-5802 | Sodium Chloride | SODIUM CHLORIDE |
| 0264-5804 | Sodium Chloride | SODIUM CHLORIDE |
| 0264-7800 | Sodium Chloride | Sodium Chloride |
| 0264-7802 | Sodium Chloride | SODIUM CHLORIDE |
| 0264-7805 | Sodium Chloride | Sodium Chloride |
| 0264-7806 | Sodium Chloride | Sodium Chloride |
| 0264-9375 | Sodium Chloride | Sodium Chloride |
| 0264-9999 | Sodium Chloride | Sodium Chloride |
| 0338-0043 | Sodium Chloride | Sodium Chloride |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CLEANOZ 78706949 3235195 Live/Registered |
UBIMED INC. 2005-09-06 |
![]() CLEANOZ 77562084 3605651 Dead/Cancelled |
UBIMED INC. 2008-09-04 |