| Product NDC: | 52380-1738 |
| Proprietary Name: | Aplicare Povidone Iodine |
| Non Proprietary Name: | Povidone Iodine |
| Active Ingredient(s): | 10 g/100g & nbsp; Povidone Iodine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52380-1738 |
| Labeler Name: | Aplicare, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19980901 |
| Package NDC: | 52380-1738-4 |
| Package Description: | 120 g in 1 BOTTLE (52380-1738-4) |
| NDC Code | 52380-1738-4 |
| Proprietary Name | Aplicare Povidone Iodine |
| Package Description | 120 g in 1 BOTTLE (52380-1738-4) |
| Product NDC | 52380-1738 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Povidone Iodine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19980901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aplicare, Inc. |
| Substance Name | POVIDONE-IODINE |
| Strength Number | 10 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |