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 |