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Antiseptic
Antiseptic - 47682-214-71 - (benzalkonium chloride)
Drug Information of Antiseptic
| Product NDC: | 47682-214 |
| Proprietary Name: | Antiseptic |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | 1.3 mg/mL & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antiseptic
| Product NDC: | 47682-214 |
| Labeler Name: | Unifirst First Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120222 |
Package Information of Antiseptic
| Package NDC: | 47682-214-71 |
| Package Description: | 20 PACKET in 1 BOX (47682-214-71) > 2.5 mL in 1 PACKET (47682-214-99) |
NDC Information of Antiseptic
| NDC Code | 47682-214-71 |
| Proprietary Name | Antiseptic |
| Package Description | 20 PACKET in 1 BOX (47682-214-71) > 2.5 mL in 1 PACKET (47682-214-99) |
| Product NDC | 47682-214 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120222 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Unifirst First Aid Corporation |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
