| Product NDC: | 17271-503 |
| Proprietary Name: | BD E-Z Scrub |
| Non Proprietary Name: | Povidone-Iodine |
| Active Ingredient(s): | 50 mg/mL & nbsp; Povidone-Iodine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17271-503 |
| Labeler Name: | Becton Dickinson and Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20000401 |
| Package NDC: | 17271-503-01 |
| Package Description: | 6 BOTTLE in 1 BOX (17271-503-01) > 946 mL in 1 BOTTLE |
| NDC Code | 17271-503-01 |
| Proprietary Name | BD E-Z Scrub |
| Package Description | 6 BOTTLE in 1 BOX (17271-503-01) > 946 mL in 1 BOTTLE |
| Product NDC | 17271-503 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Povidone-Iodine |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20000401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Becton Dickinson and Company |
| Substance Name | POVIDONE-IODINE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |