Product NDC: | 0395-1213 |
Proprietary Name: | Iodine Tincture Mild |
Non Proprietary Name: | Iodine and Sodium Iodide and Alcohol |
Active Ingredient(s): | 470; 20; 20.4 mg/mL; mg/mL; mg/mL & nbsp; Iodine and Sodium Iodide and Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0395-1213 |
Labeler Name: | Humco Holding Group, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19790101 |
Package NDC: | 0395-1213-91 |
Package Description: | 30 mL in 1 BOTTLE (0395-1213-91) |
NDC Code | 0395-1213-91 |
Proprietary Name | Iodine Tincture Mild |
Package Description | 30 mL in 1 BOTTLE (0395-1213-91) |
Product NDC | 0395-1213 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Iodine and Sodium Iodide and Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19790101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Humco Holding Group, Inc |
Substance Name | ALCOHOL; IODINE; SODIUM IODIDE |
Strength Number | 470; 20; 20.4 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |