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) |
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 NDC: | 54365-400-14 |
Package Description: | 1 APPLICATOR in 1 POUCH (54365-400-14) > 26 mL in 1 APPLICATOR |
NDC Code | 54365-400-14 |
Proprietary Name | ChloraPrep One-Step |
Package Description | 1 APPLICATOR in 1 POUCH (54365-400-14) > 26 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 |