Product NDC: | 47682-244 |
Proprietary Name: | Antiseptic |
Non Proprietary Name: | benzalkonium chloride, benzocaine |
Active Ingredient(s): | .96; 58.5 g/L; g/L & nbsp; benzalkonium chloride, benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47682-244 |
Labeler Name: | Unifirst First Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130412 |
Package NDC: | 47682-244-17 |
Package Description: | .09 L in 1 BOTTLE, SPRAY (47682-244-17) |
NDC Code | 47682-244-17 |
Proprietary Name | Antiseptic |
Package Description | .09 L in 1 BOTTLE, SPRAY (47682-244-17) |
Product NDC | 47682-244 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzalkonium chloride, benzocaine |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20130412 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Unifirst First Aid Corporation |
Substance Name | BENZALKONIUM CHLORIDE; BENZOCAINE |
Strength Number | .96; 58.5 |
Strength Unit | g/L; g/L |
Pharmaceutical Classes |