Drug Details: HIBICLENS

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HIBICLENS
FDA Application No:	(NDA) 018423
Active Ingredient(s):	CHLORHEXIDINE GLUCONATE
Company:	REGENT
Original Approval or Tentative Approval Date:	August 27, 1981
Chemical Type:	5 New manufacturer
Review Classification:	S Standard review drug

Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
HIBICLENS	CHLORHEXIDINE GLUCONATE	4%	SPONGE; TOPICAL	OTC	Yes	None

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