| Product NDC: | 52000-008 |
| Proprietary Name: | Isopropyl Rubbing Alcohol 50% |
| 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: | 52000-008 |
| Labeler Name: | Universal Distribution Center LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120313 |
| Package NDC: | 52000-008-05 |
| Package Description: | 355 mL in 1 BOTTLE, PLASTIC (52000-008-05) |
| NDC Code | 52000-008-05 |
| Proprietary Name | Isopropyl Rubbing Alcohol 50% |
| Package Description | 355 mL in 1 BOTTLE, PLASTIC (52000-008-05) |
| Product NDC | 52000-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Isopropyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120313 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Universal Distribution Center LLC |
| Substance Name | ISOPROPYL ALCOHOL |
| Strength Number | 50 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |