| Product NDC: | 49348-030 |
| Proprietary Name: | sunmark Isopropyl Rubbing Alcohol |
| Non Proprietary Name: | ISOPROPYL ALCOHOL |
| Active Ingredient(s): | 70 L/100L & nbsp; ISOPROPYL ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49348-030 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120628 |
| Package NDC: | 49348-030-40 |
| Package Description: | 3.8 L in 1 BOTTLE (49348-030-40) |
| NDC Code | 49348-030-40 |
| Proprietary Name | sunmark Isopropyl Rubbing Alcohol |
| Package Description | 3.8 L in 1 BOTTLE (49348-030-40) |
| Product NDC | 49348-030 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ISOPROPYL ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120628 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | ISOPROPYL ALCOHOL |
| Strength Number | 70 |
| Strength Unit | L/100L |
| Pharmaceutical Classes |