Home
>
National Drug Code (NDC)
>
Kay Foaming Hand Sanitizer
Kay Foaming Hand Sanitizer - 63146-109-03 - (Benzalkonium Chloride)
Drug Information of Kay Foaming Hand Sanitizer
| Product NDC: | 63146-109 |
| Proprietary Name: | Kay Foaming Hand Sanitizer |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .1 mL/100mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kay Foaming Hand Sanitizer
| Product NDC: | 63146-109 |
| Labeler Name: | Kay Chemical Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080222 |
Package Information of Kay Foaming Hand Sanitizer
| Package NDC: | 63146-109-03 |
| Package Description: | 750 mL in 1 BOTTLE, PLASTIC (63146-109-03) |
NDC Information of Kay Foaming Hand Sanitizer
| NDC Code | 63146-109-03 |
| Proprietary Name | Kay Foaming Hand Sanitizer |
| Package Description | 750 mL in 1 BOTTLE, PLASTIC (63146-109-03) |
| Product NDC | 63146-109 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20080222 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kay Chemical Company |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
