| Product NDC: | 59365-6064 |
| Proprietary Name: | Lugols Strong Iodine |
| Non Proprietary Name: | Iodine Potassium Iodide |
| Active Ingredient(s): | .05; .105 g/mL; g/mL & nbsp; Iodine Potassium Iodide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59365-6064 |
| Labeler Name: | CooperSurgical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19921001 |
| Package NDC: | 59365-6064-1 |
| Package Description: | 12 VIAL, SINGLE-USE in 1 CARTON (59365-6064-1) > 8 mL in 1 VIAL, SINGLE-USE |
| NDC Code | 59365-6064-1 |
| Proprietary Name | Lugols Strong Iodine |
| Package Description | 12 VIAL, SINGLE-USE in 1 CARTON (59365-6064-1) > 8 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 59365-6064 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Iodine Potassium Iodide |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19921001 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CooperSurgical, Inc. |
| Substance Name | IODINE; POTASSIUM IODIDE |
| Strength Number | .05; .105 |
| Strength Unit | g/mL; g/mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |