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ChloraPrep One-Step
ChloraPrep One-Step - 54365-400-07 - (chlorhexidine gluconate and isopropyl aclohol)
Drug Information of ChloraPrep One-Step
| Product NDC: | 54365-400 |
| Proprietary Name: | ChloraPrep One-Step |
| Non Proprietary Name: | chlorhexidine gluconate and isopropyl aclohol |
| Active Ingredient(s): | 20; .7 mg/mL; mL/mL & nbsp; chlorhexidine gluconate and isopropyl aclohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ChloraPrep One-Step
| Product NDC: | 54365-400 |
| Labeler Name: | CareFusion 213 LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020832 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060818 |
Package Information of ChloraPrep One-Step
| Package NDC: | 54365-400-07 |
| Package Description: | 48 POUCH in 1 CARTON (54365-400-07) > 1 APPLICATOR in 1 POUCH > 1.75 mL in 1 APPLICATOR |
NDC Information of ChloraPrep One-Step
| NDC Code | 54365-400-07 |
| Proprietary Name | ChloraPrep One-Step |
| Package Description | 48 POUCH in 1 CARTON (54365-400-07) > 1 APPLICATOR in 1 POUCH > 1.75 mL in 1 APPLICATOR |
| Product NDC | 54365-400 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | chlorhexidine gluconate and isopropyl aclohol |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060818 |
| Marketing Category Name | NDA |
| Labeler Name | CareFusion 213 LLC |
| Substance Name | CHLORHEXIDINE GLUCONATE; ISOPROPYL ALCOHOL |
| Strength Number | 20; .7 |
| Strength Unit | mg/mL; mL/mL |
| Pharmaceutical Classes |
