| 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 |