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Peridex
Peridex - 48878-0620-4 - (chlorhexidine gluconate)
Drug Information of Peridex
| Product NDC: | 48878-0620 |
| Proprietary Name: | Peridex |
| Non Proprietary Name: | chlorhexidine gluconate |
| Active Ingredient(s): | 1.2 mg/mL & nbsp; chlorhexidine gluconate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Peridex
| Product NDC: | 48878-0620 |
| Labeler Name: | 3M ESPE Dental Products |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019028 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19860813 |
Package Information of Peridex
| Package NDC: | 48878-0620-4 |
| Package Description: | 15 mL in 1 BOTTLE (48878-0620-4) |
NDC Information of Peridex
| NDC Code | 48878-0620-4 |
| Proprietary Name | Peridex |
| Package Description | 15 mL in 1 BOTTLE (48878-0620-4) |
| Product NDC | 48878-0620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlorhexidine gluconate |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 19860813 |
| Marketing Category Name | NDA |
| Labeler Name | 3M ESPE Dental Products |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | 1.2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Cell Wall Integrity [PE] |
