Product NDC: | 65517-0004 |
Proprietary Name: | BZK Towelette |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | .00186 mL/1.4mL & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SWAB |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65517-0004 |
Labeler Name: | DUKAL CORPORATION |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20060101 |
Package NDC: | 65517-0004-1 |
Package Description: | 1.4 mL in 1 POUCH (65517-0004-1) |
NDC Code | 65517-0004-1 |
Proprietary Name | BZK Towelette |
Package Description | 1.4 mL in 1 POUCH (65517-0004-1) |
Product NDC | 65517-0004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | SWAB |
Route Name | TOPICAL |
Start Marketing Date | 20060101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DUKAL CORPORATION |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .00186 |
Strength Unit | mL/1.4mL |
Pharmaceutical Classes |