Home
>
National Drug Code (NDC)
>
Antibacterial Hand
Antibacterial Hand - 76268-001-01 - (Benzalkonium Chloride)
Drug Information of Antibacterial Hand
| Product NDC: | 76268-001 |
| Proprietary Name: | Antibacterial Hand |
| 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 Antibacterial Hand
| Product NDC: | 76268-001 |
| Labeler Name: | ORGANICA (UK) LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110727 |
Package Information of Antibacterial Hand
| Package NDC: | 76268-001-01 |
| Package Description: | 50 mL in 1 BOTTLE, PLASTIC (76268-001-01) |
NDC Information of Antibacterial Hand
| NDC Code | 76268-001-01 |
| Proprietary Name | Antibacterial Hand |
| Package Description | 50 mL in 1 BOTTLE, PLASTIC (76268-001-01) |
| Product NDC | 76268-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ORGANICA (UK) LTD |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
