Home
>
National Drug Code (NDC)
>
BZK Towelette
BZK Towelette - 65517-0004-1 - (BENZALKONIUM CHLORIDE)
Drug Information of BZK Towelette
| 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) |
Labeler Information of BZK Towelette
| 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 Information of BZK Towelette
| Package NDC: | 65517-0004-1 |
| Package Description: | 1.4 mL in 1 POUCH (65517-0004-1) |
NDC Information of BZK Towelette
| 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 |
