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Antibacterial Foaming Hand
Antibacterial Foaming Hand - 42961-001-06 - (Benzalkonium Chloride)
Drug Information of Antibacterial Foaming Hand
| Product NDC: | 42961-001 |
| Proprietary Name: | Antibacterial Foaming Hand |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | 1.25 mg/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antibacterial Foaming Hand
| Product NDC: | 42961-001 |
| Labeler Name: | Cintas Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080422 |
Package Information of Antibacterial Foaming Hand
| Package NDC: | 42961-001-06 |
| Package Description: | 50 mL in 1 BOTTLE, PLASTIC (42961-001-06) |
NDC Information of Antibacterial Foaming Hand
| NDC Code | 42961-001-06 |
| Proprietary Name | Antibacterial Foaming Hand |
| Package Description | 50 mL in 1 BOTTLE, PLASTIC (42961-001-06) |
| Product NDC | 42961-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20080422 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cintas Corp. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
