Product NDC: | 59294-001 |
Proprietary Name: | Alcohol Prep Pad |
Non Proprietary Name: | ISOPROPYL ALCOHOL |
Active Ingredient(s): | 70 g/100g & nbsp; ISOPROPYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59294-001 |
Labeler Name: | Global Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130711 |
Package NDC: | 59294-001-00 |
Package Description: | 1 PATCH in 1 PACKET (59294-001-00) > .9 g in 1 PATCH |
NDC Code | 59294-001-00 |
Proprietary Name | Alcohol Prep Pad |
Package Description | 1 PATCH in 1 PACKET (59294-001-00) > .9 g in 1 PATCH |
Product NDC | 59294-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ISOPROPYL ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130711 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Global Healthcare |
Substance Name | ISOPROPYL ALCOHOL |
Strength Number | 70 |
Strength Unit | g/100g |
Pharmaceutical Classes |