Visitor Monitoring Drug History: OCUCLEAR
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: OCUCLEAR
FDA Application No: (NDA) 018471
Active Ingredient(s): OXYMETAZOLINE HYDROCHLORIDE
Company: SCHERING PLOUGH
 
Label History
 
Labels are not available on this site for OCUCLEAR, (NDA) 018471
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/6/2001 016Control Supplement  
1/24/2001 015Control Supplement  
7/14/1997 014Control Supplement  
11/13/1996 013Manufacturing Change or Addition  
5/16/1990 012Control Supplement  
8/24/1989 011Labeling Revision  
4/6/1989 008Package Change  
6/9/1989 007Manufacturing Change or Addition  
3/30/1989 006Control Supplement  
1/15/1988 005Control Supplement  
8/4/1987 004Manufacturing Change or Addition  
5/12/1987 003Manufacturing Change or Addition  
8/3/1987 002Control Supplement  
8/20/1986 001Manufacturing Change or Addition  
5/30/1986 000Approval  
 
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