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KIMVENT
KIMVENT - 55118-976-01 - (Chlorhexidine Gluconate and Hydrogen Peroxide)
Drug Information of KIMVENT
| Product NDC: | 55118-976 |
| Proprietary Name: | KIMVENT |
| Non Proprietary Name: | Chlorhexidine Gluconate and Hydrogen Peroxide |
| Active Ingredient(s): | & nbsp; Chlorhexidine Gluconate and Hydrogen Peroxide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KIMVENT
| Product NDC: | 55118-976 |
| Labeler Name: | Kimberly-Clark Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074356 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960507 |
Package Information of KIMVENT
| Package NDC: | 55118-976-01 |
| Package Description: | 1 KIT in 1 CARTON (55118-976-01) * 14 mL in 1 CUP, UNIT-DOSE * 10 g in 1 TUBE * 15 mL in 1 CUP, UNIT-DOSE |
NDC Information of KIMVENT
| NDC Code | 55118-976-01 |
| Proprietary Name | KIMVENT |
| Package Description | 1 KIT in 1 CARTON (55118-976-01) * 14 mL in 1 CUP, UNIT-DOSE * 10 g in 1 TUBE * 15 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 55118-976 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorhexidine Gluconate and Hydrogen Peroxide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19960507 |
| Marketing Category Name | ANDA |
| Labeler Name | Kimberly-Clark Corporation |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
