| Product NDC: | 10565-013 |
| Proprietary Name: | Alcohol |
| Non Proprietary Name: | Isopropyl Alcohol |
| Active Ingredient(s): | 62 mL/100mL & nbsp; Isopropyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10565-013 |
| Labeler Name: | Hydrox Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111205 |
| Package NDC: | 10565-013-02 |
| Package Description: | 59 mL in 1 BOTTLE, PLASTIC (10565-013-02) |
| NDC Code | 10565-013-02 |
| Proprietary Name | Alcohol |
| Package Description | 59 mL in 1 BOTTLE, PLASTIC (10565-013-02) |
| Product NDC | 10565-013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Isopropyl Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20111205 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Hydrox Laboratories |
| Substance Name | ISOPROPYL ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |