Product NDC: | 52759-922 |
Proprietary Name: | Oosafe |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | 1.3 g/L & nbsp; Benzalkonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52759-922 |
Labeler Name: | SPARMED ApS |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120430 |
Package NDC: | 52759-922-00 |
Package Description: | .25 L in 1 BOTTLE (52759-922-00) |
NDC Code | 52759-922-00 |
Proprietary Name | Oosafe |
Package Description | .25 L in 1 BOTTLE (52759-922-00) |
Product NDC | 52759-922 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120430 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SPARMED ApS |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | 1.3 |
Strength Unit | g/L |
Pharmaceutical Classes |