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Povidone Iodine
Povidone Iodine - 49738-050-34 - (povidone-iodine)
Drug Information of Povidone Iodine
| Product NDC: | 49738-050 |
| Proprietary Name: | Povidone Iodine |
| Non Proprietary Name: | povidone-iodine |
| Active Ingredient(s): | .1 mg/mL & nbsp; povidone-iodine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Povidone Iodine
| Product NDC: | 49738-050 |
| Labeler Name: | Kmart Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060913 |
Package Information of Povidone Iodine
| Package NDC: | 49738-050-34 |
| Package Description: | 236 mL in 1 BOTTLE (49738-050-34) |
NDC Information of Povidone Iodine
| NDC Code | 49738-050-34 |
| Proprietary Name | Povidone Iodine |
| Package Description | 236 mL in 1 BOTTLE (49738-050-34) |
| Product NDC | 49738-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | povidone-iodine |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060913 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kmart Corporation |
| Substance Name | POVIDONE-IODINE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
