Product NDC: | 68345-883 |
Proprietary Name: | Benzalkonium Chloride Towelette |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | .13 g/100g & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68345-883 |
Labeler Name: | PSS World Medical, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130620 |
Package NDC: | 68345-883-50 |
Package Description: | 10 BOX in 1 CASE (68345-883-50) > 100 PACKET in 1 BOX > 1.5 g in 1 PACKET |
NDC Code | 68345-883-50 |
Proprietary Name | Benzalkonium Chloride Towelette |
Package Description | 10 BOX in 1 CASE (68345-883-50) > 100 PACKET in 1 BOX > 1.5 g in 1 PACKET |
Product NDC | 68345-883 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130620 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | PSS World Medical, Inc. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .13 |
Strength Unit | g/100g |
Pharmaceutical Classes |