| Product NDC: | 54365-200 |
| Proprietary Name: | Blood Culture Prep Kit |
| Non Proprietary Name: | Isopropyl alcohol and iodine |
| Active Ingredient(s): | & nbsp; Isopropyl alcohol and iodine |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54365-200 |
| Labeler Name: | CareFusion 213 LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19880201 |
| Package NDC: | 54365-200-99 |
| Package Description: | 1 KIT in 1 POUCH (54365-200-99) * 1.1 mL in 1 APPLICATOR (54365-170-02) * .67 mL in 1 AMPULE (54365-161-01) |
| NDC Code | 54365-200-99 |
| Proprietary Name | Blood Culture Prep Kit |
| Package Description | 1 KIT in 1 POUCH (54365-200-99) * 1.1 mL in 1 APPLICATOR (54365-170-02) * .67 mL in 1 AMPULE (54365-161-01) |
| Product NDC | 54365-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Isopropyl alcohol and iodine |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19880201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CareFusion 213 LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |