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Zaliex Alcohol-Free Foaming Hand Sanitizer
Zaliex Alcohol-Free Foaming Hand Sanitizer - 76452-004-00 - (BENZALKONIUM CHLORIDE)
Drug Information of Zaliex Alcohol-Free Foaming Hand Sanitizer
| Product NDC: | 76452-004 |
| Proprietary Name: | Zaliex Alcohol-Free Foaming Hand Sanitizer |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .1 mg/.001L & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zaliex Alcohol-Free Foaming Hand Sanitizer
| Product NDC: | 76452-004 |
| Labeler Name: | SAS Healthcare Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111026 |
Package Information of Zaliex Alcohol-Free Foaming Hand Sanitizer
| Package NDC: | 76452-004-00 |
| Package Description: | 1 L in 1 BOTTLE (76452-004-00) |
NDC Information of Zaliex Alcohol-Free Foaming Hand Sanitizer
| NDC Code | 76452-004-00 |
| Proprietary Name | Zaliex Alcohol-Free Foaming Hand Sanitizer |
| Package Description | 1 L in 1 BOTTLE (76452-004-00) |
| Product NDC | 76452-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111026 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SAS Healthcare Inc |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mg/.001L |
| Pharmaceutical Classes |
