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Celox Ultra
Celox Ultra - 75990-007-10 - (ALCOHOL)
Drug Information of Celox Ultra
| Product NDC: | 75990-007 |
| Proprietary Name: | Celox Ultra |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Celox Ultra
| Product NDC: | 75990-007 |
| Labeler Name: | Certus Medical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110425 |
Package Information of Celox Ultra
| Package NDC: | 75990-007-10 |
| Package Description: | 1000 mL in 1 CARTRIDGE (75990-007-10) |
NDC Information of Celox Ultra
| NDC Code | 75990-007-10 |
| Proprietary Name | Celox Ultra |
| Package Description | 1000 mL in 1 CARTRIDGE (75990-007-10) |
| Product NDC | 75990-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110425 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Certus Medical, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
