Product NDC: | 35418-203 |
Proprietary Name: | Alcohol Prep pad |
Non Proprietary Name: | Isopropyl Alcohol |
Active Ingredient(s): | .7 mL/mL & nbsp; Isopropyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SWAB |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35418-203 |
Labeler Name: | ZEE MEDICAL |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part344 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130115 |
Package NDC: | 35418-203-01 |
Package Description: | 50 POUCH in 1 BOX (35418-203-01) > 1 mL in 1 POUCH |
NDC Code | 35418-203-01 |
Proprietary Name | Alcohol Prep pad |
Package Description | 50 POUCH in 1 BOX (35418-203-01) > 1 mL in 1 POUCH |
Product NDC | 35418-203 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Isopropyl Alcohol |
Dosage Form Name | SWAB |
Route Name | TOPICAL |
Start Marketing Date | 20130115 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | ZEE MEDICAL |
Substance Name | ISOPROPYL ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |