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FOAMING HAND SANITIZER
FOAMING HAND SANITIZER - 36800-240-08 - (BENZALKONIUM CHLORIDE)
Drug Information of FOAMING HAND SANITIZER
| Product NDC: | 36800-240 |
| 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): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FOAMING HAND SANITIZER
| Product NDC: | 36800-240 |
| Labeler Name: | TOPCO ASSOCIATES LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110623 |
Package Information of FOAMING HAND SANITIZER
| Package NDC: | 36800-240-08 |
| Package Description: | 236 mL in 1 BOTTLE (36800-240-08) |
NDC Information of FOAMING HAND SANITIZER
| NDC Code | 36800-240-08 |
| Proprietary Name | FOAMING HAND SANITIZER |
| Package Description | 236 mL in 1 BOTTLE (36800-240-08) |
| Product NDC | 36800-240 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110623 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TOPCO ASSOCIATES LLC |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
