ChloraPrep One-Step is a Topical Solution in the Human Otc Drug category. It is labeled and distributed by Carefusion 213 Llc. The primary component is Chlorhexidine Gluconate; Isopropyl Alcohol.
| Product ID | 54365-400_7cb2fbbd-5562-4ced-e053-2991aa0afa8d |
| NDC | 54365-400 |
| Product Type | Human Otc Drug |
| Proprietary Name | ChloraPrep One-Step |
| Generic Name | Chlorhexidine Gluconate And Isopropyl Alcohol |
| Dosage Form | Solution |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2000-07-14 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020832 |
| Labeler Name | CareFusion 213 LLC |
| Substance Name | CHLORHEXIDINE GLUCONATE; ISOPROPYL ALCOHOL |
| Active Ingredient Strength | 20 mg/mL; mL/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2009-06-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA021555 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-05-10 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2002-04-26 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-07-14 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA021555 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2002-10-07 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2006-08-18 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-07-23 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2006-08-18 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-01-07 |
| Marketing End Date | 2014-01-23 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2002-04-26 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2006-08-18 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-07-14 |
| Marketing Category | NDA |
| Application Number | NDA021555 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-06-10 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2002-04-26 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-05-24 |
| Marketing Category | NDA |
| Application Number | NDA020832 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-07-14 |
| Ingredient | Strength |
|---|---|
| CHLORHEXIDINE GLUCONATE | 20 mg/mL |
| SPL SET ID: | 3f94d971-0d96-47a2-9117-540dfd1278a6 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 54365-400 | ChloraPrep One-Step | chlorhexidine gluconate and isopropyl alcohol |
| 17518-080 | 3M SoluPrep | chlorhexidine gluconate and isopropyl alcohol |
| 17518-081 | 3M SoluPrep | chlorhexidine gluconate and isopropyl alcohol |
| 0234-0587 | Hibistat | Chlorhexidine gluconate and Isopropyl alcohol |
| 10819-4075 | Prevantics Maxi Swabstick | chlorhexidine gluconate and isopropyl alcohol |
| 10819-4076 | Prevantics Maxi Swabstick | chlorhexidine gluconate and isopropyl alcohol |
| 10819-1080 | Prevantics Swab | Chlorhexidine Gluconate and Isopropyl Alcohol |
| 10819-4077 | Prevantics Swabstick | chlorhexidine gluconate and isopropyl alcohol |