Product NDC: | 34954-008 |
Proprietary Name: | ISOPROPYL RUBBING ALCOHOL |
Non Proprietary Name: | ISOPROPYL ALCOHOL |
Active Ingredient(s): | 50 mL/100mL & nbsp; ISOPROPYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 34954-008 |
Labeler Name: | KIM CHEMICALS LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091001 |
Package NDC: | 34954-008-12 |
Package Description: | 355 mL in 1 BOTTLE, PLASTIC (34954-008-12) |
NDC Code | 34954-008-12 |
Proprietary Name | ISOPROPYL RUBBING ALCOHOL |
Package Description | 355 mL in 1 BOTTLE, PLASTIC (34954-008-12) |
Product NDC | 34954-008 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ISOPROPYL ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20091001 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | KIM CHEMICALS LTD. |
Substance Name | ISOPROPYL ALCOHOL |
Strength Number | 50 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |