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BZK
BZK - 0404-6735-01 - (benzalkonium chloride)
Drug Information of BZK
| Product NDC: | 0404-6735 |
| Proprietary Name: | BZK |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | .0013 g/g & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BZK
| Product NDC: | 0404-6735 |
| Labeler Name: | Henry Schein Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130107 |
Package Information of BZK
| Package NDC: | 0404-6735-01 |
| Package Description: | 100 PACKET in 1 BOX (0404-6735-01) > 2.5 g in 1 PACKET |
NDC Information of BZK
| NDC Code | 0404-6735-01 |
| Proprietary Name | BZK |
| Package Description | 100 PACKET in 1 BOX (0404-6735-01) > 2.5 g in 1 PACKET |
| Product NDC | 0404-6735 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130107 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Henry Schein Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .0013 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
