Product NDC: | 47682-302 |
Proprietary Name: | Antiseptic |
Non Proprietary Name: | benzalkonium chloride |
Active Ingredient(s): | 1.3 mg/g & nbsp; benzalkonium chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47682-302 |
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 NDC: | 47682-302-73 |
Package Description: | 25 PACKET in 1 BOX (47682-302-73) > 2.5 g in 1 PACKET |
NDC Code | 47682-302-73 |
Proprietary Name | Antiseptic |
Package Description | 25 PACKET in 1 BOX (47682-302-73) > 2.5 g in 1 PACKET |
Product NDC | 47682-302 |
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/g |
Pharmaceutical Classes |