Product NDC: | 12745-105 |
Proprietary Name: | Isopropyl Alcohol |
Non Proprietary Name: | Isopropyl Alcohol |
Active Ingredient(s): | 70.14 g/100mL & nbsp; Isopropyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 12745-105 |
Labeler Name: | Medical Chemical Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part344 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19540615 |
Package NDC: | 12745-105-05 |
Package Description: | 18927 mL in 1 CONTAINER (12745-105-05) |
NDC Code | 12745-105-05 |
Proprietary Name | Isopropyl Alcohol |
Package Description | 18927 mL in 1 CONTAINER (12745-105-05) |
Product NDC | 12745-105 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Isopropyl Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19540615 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medical Chemical Corporation |
Substance Name | ISOPROPYL ALCOHOL |
Strength Number | 70.14 |
Strength Unit | g/100mL |
Pharmaceutical Classes |