Visitor Monitoring Drug History: HIBICLENS
 
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: HIBICLENS
FDA Application No: (NDA) 018423
Active Ingredient(s): CHLORHEXIDINE GLUCONATE
Company: REGENT
 
Label History
 
Labels are not available on this site for HIBICLENS, (NDA) 018423
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/12/2001 016Manufacturing Change or Addition  
10/19/1999 014Package Change  
7/23/1992 013Control Supplement  
7/14/1989 012Formulation Revision  
9/15/1989 011Control Supplement  
8/25/1989 010Labeling Revision  
7/5/1988 008Manufacturing Change or Addition  
6/22/1988 007Labeling Revision  
12/10/1987 006Manufacturing Change or Addition  
9/2/1988 005Control Supplement  
2/22/1986 003Control Supplement  
11/18/1983 002Control Supplement  
10/19/1981 001Control Supplement  
8/27/1981 000Approval  
 
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