Product NDC: | 28691-1234 |
Proprietary Name: | Alcohol swab |
Non Proprietary Name: | Alcohol swab |
Active Ingredient(s): | .7 mL/mL & nbsp; Alcohol swab |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SWAB |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 28691-1234 |
Labeler Name: | Pharmaplast SAE |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20070101 |
Package NDC: | 28691-1234-1 |
Package Description: | 1 mL in 1 PACKET (28691-1234-1) |
NDC Code | 28691-1234-1 |
Proprietary Name | Alcohol swab |
Package Description | 1 mL in 1 PACKET (28691-1234-1) |
Product NDC | 28691-1234 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol swab |
Dosage Form Name | SWAB |
Route Name | TOPICAL |
Start Marketing Date | 20070101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Pharmaplast SAE |
Substance Name | ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |