Product NDC: | 17518-011 |
Proprietary Name: | 3M DuraPrep Surgical |
Non Proprietary Name: | Iodine povacrylex and Isopropyl alcohol |
Active Ingredient(s): | 6.02; 636.4 mg/mL; mg/mL & nbsp; Iodine povacrylex and Isopropyl alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17518-011 |
Labeler Name: | 3M Health Care |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021586 |
Marketing Category: | NDA |
Start Marketing Date: | 20060929 |
Package NDC: | 17518-011-07 |
Package Description: | 50 APPLICATOR in 1 CASE (17518-011-07) > 6 mL in 1 APPLICATOR |
NDC Code | 17518-011-07 |
Proprietary Name | 3M DuraPrep Surgical |
Package Description | 50 APPLICATOR in 1 CASE (17518-011-07) > 6 mL in 1 APPLICATOR |
Product NDC | 17518-011 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Iodine povacrylex and Isopropyl alcohol |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20060929 |
Marketing Category Name | NDA |
Labeler Name | 3M Health Care |
Substance Name | IODINE POVACRYLEX; ISOPROPYL ALCOHOL |
Strength Number | 6.02; 636.4 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |