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Sunmark Iodine
Sunmark Iodine - 49348-133-27 - (IODINE, SODIUM IODIDE, ALCOHOL)
Drug Information of Sunmark Iodine
| Product NDC: | 49348-133 |
| Proprietary Name: | Sunmark Iodine |
| Non Proprietary Name: | IODINE, SODIUM IODIDE, ALCOHOL |
| Active Ingredient(s): | 470; 20; 20.4 mg/mL; mg/mL; mg/mL & nbsp; IODINE, SODIUM IODIDE, ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | TINCTURE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Iodine
| Product NDC: | 49348-133 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120628 |
Package Information of Sunmark Iodine
| Package NDC: | 49348-133-27 |
| Package Description: | 30 mL in 1 BOTTLE (49348-133-27) |
NDC Information of Sunmark Iodine
| NDC Code | 49348-133-27 |
| Proprietary Name | Sunmark Iodine |
| Package Description | 30 mL in 1 BOTTLE (49348-133-27) |
| Product NDC | 49348-133 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IODINE, SODIUM IODIDE, ALCOHOL |
| Dosage Form Name | TINCTURE |
| Route Name | TOPICAL |
| Start Marketing Date | 20120628 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | ALCOHOL; IODINE; SODIUM IODIDE |
| Strength Number | 470; 20; 20.4 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
