Product NDC: | 49348-622 |
Proprietary Name: | sunmark Povidone-Iodine Topical |
Non Proprietary Name: | POVIDONE-IODINE |
Active Ingredient(s): | 100 mg/mL & nbsp; POVIDONE-IODINE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-622 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120628 |
Package NDC: | 49348-622-37 |
Package Description: | 237 mL in 1 BOTTLE (49348-622-37) |
NDC Code | 49348-622-37 |
Proprietary Name | sunmark Povidone-Iodine Topical |
Package Description | 237 mL in 1 BOTTLE (49348-622-37) |
Product NDC | 49348-622 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | POVIDONE-IODINE |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20120628 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | POVIDONE-IODINE |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes |