Home
>
National Drug Code (NDC)
>
Decolorized Iodine
Decolorized Iodine - 37205-648-16 - (Ethyl Alcohol)
Drug Information of Decolorized Iodine
| Product NDC: | 37205-648 |
| Proprietary Name: | Decolorized Iodine |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | .45 mL/mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Decolorized Iodine
| Product NDC: | 37205-648 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19790101 |
Package Information of Decolorized Iodine
| Package NDC: | 37205-648-16 |
| Package Description: | 59 mL in 1 BOTTLE (37205-648-16) |
NDC Information of Decolorized Iodine
| NDC Code | 37205-648-16 |
| Proprietary Name | Decolorized Iodine |
| Package Description | 59 mL in 1 BOTTLE (37205-648-16) |
| Product NDC | 37205-648 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 19790101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cardinal Health |
| Substance Name | ALCOHOL |
| Strength Number | .45 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
