Home
>
National Drug Code (NDC)
>
FOAMING HAND SANITIZER
FOAMING HAND SANITIZER - 37808-240-08 - (BENZALKONIUM CHLORIDE)
Drug Information of FOAMING HAND SANITIZER
| Product NDC: | 37808-240 |
| Proprietary Name: | FOAMING HAND SANITIZER |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .1 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FOAMING HAND SANITIZER
| Product NDC: | 37808-240 |
| Labeler Name: | HEB |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100714 |
Package Information of FOAMING HAND SANITIZER
| Package NDC: | 37808-240-08 |
| Package Description: | 236 mL in 1 BOTTLE, PUMP (37808-240-08) |
NDC Information of FOAMING HAND SANITIZER
| NDC Code | 37808-240-08 |
| Proprietary Name | FOAMING HAND SANITIZER |
| Package Description | 236 mL in 1 BOTTLE, PUMP (37808-240-08) |
| Product NDC | 37808-240 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100714 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | HEB |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
