Oosafe - 52759-922-00 - (Benzalkonium Chloride)

Alphabetical Index


Drug Information of Oosafe

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)

Labeler Information of Oosafe

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 Information of Oosafe

Package NDC: 52759-922-00
Package Description: .25 L in 1 BOTTLE (52759-922-00)

NDC Information of Oosafe

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

Complete Information of Oosafe


General Information