| Product NDC: | 10819-3890 |
| Proprietary Name: | PDI Duo-Swab Povidone-Iodine |
| Non Proprietary Name: | Povidone Iodine |
| Active Ingredient(s): | .1 mL/mL & nbsp; Povidone Iodine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10819-3890 |
| Labeler Name: | Professional Disposables International, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19780101 |
| Package NDC: | 10819-3890-1 |
| Package Description: | 5 mL in 1 PACKET (10819-3890-1) |
| NDC Code | 10819-3890-1 |
| Proprietary Name | PDI Duo-Swab Povidone-Iodine |
| Package Description | 5 mL in 1 PACKET (10819-3890-1) |
| Product NDC | 10819-3890 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Povidone Iodine |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 19780101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Professional Disposables International, Inc. |
| Substance Name | POVIDONE-IODINE |
| Strength Number | .1 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |