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E3 Foaming Hand Sanitizer Problend
E3 Foaming Hand Sanitizer Problend - 76250-110-01 - (benzalkonium chloride)
Drug Information of E3 Foaming Hand Sanitizer Problend
| Product NDC: | 76250-110 |
| Proprietary Name: | E3 Foaming Hand Sanitizer Problend |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | 1 g/1000mL & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of E3 Foaming Hand Sanitizer Problend
| Product NDC: | 76250-110 |
| Labeler Name: | Seatex Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130508 |
Package Information of E3 Foaming Hand Sanitizer Problend
| Package NDC: | 76250-110-01 |
| Package Description: | 3780 mL in 1 BOTTLE, PLASTIC (76250-110-01) |
NDC Information of E3 Foaming Hand Sanitizer Problend
| NDC Code | 76250-110-01 |
| Proprietary Name | E3 Foaming Hand Sanitizer Problend |
| Package Description | 3780 mL in 1 BOTTLE, PLASTIC (76250-110-01) |
| Product NDC | 76250-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130508 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Seatex Ltd |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
