Home
>
National Drug Code (NDC)
>
Purgo Ultra Foam
Purgo Ultra Foam - 75990-576-55 - (TRICLOSAN)
Drug Information of Purgo Ultra Foam
| Product NDC: | 75990-576 |
| Proprietary Name: | Purgo Ultra Foam |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | 3 mg/mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Purgo Ultra Foam
| Product NDC: | 75990-576 |
| 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 Purgo Ultra Foam
| Package NDC: | 75990-576-55 |
| Package Description: | 208200 mL in 1 DRUM (75990-576-55) |
NDC Information of Purgo Ultra Foam
| NDC Code | 75990-576-55 |
| Proprietary Name | Purgo Ultra Foam |
| Package Description | 208200 mL in 1 DRUM (75990-576-55) |
| Product NDC | 75990-576 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20110425 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Certus Medical, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
