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Native Green Foaming Hand Sanitizer
Native Green Foaming Hand Sanitizer - 50409-514-82 - (benzalkonium chloride)
Drug Information of Native Green Foaming Hand Sanitizer
| Product NDC: | 50409-514 |
| Proprietary Name: | Native Green Foaming Hand Sanitizer |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | 1 g/1000mL & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Native Green Foaming Hand Sanitizer
| Product NDC: | 50409-514 |
| Labeler Name: | Native Green |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100421 |
Package Information of Native Green Foaming Hand Sanitizer
| Package NDC: | 50409-514-82 |
| Package Description: | 550 mL in 1 BOTTLE (50409-514-82) |
NDC Information of Native Green Foaming Hand Sanitizer
| NDC Code | 50409-514-82 |
| Proprietary Name | Native Green Foaming Hand Sanitizer |
| Package Description | 550 mL in 1 BOTTLE (50409-514-82) |
| Product NDC | 50409-514 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100421 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Native Green |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
