NDC Code(s) : 0023-6118-03
Packager : Allergan, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Condyloxpodofilox GEL
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0023-6118
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PODOFILOX(UNII: L36H50F353)
(PODOFILOX - UNII:L36H50F353) 		PODOFILOX5 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
ALCOHOL(UNII: 3K9958V90M)
GLYCERIN(UNII: PDC6A3C0OX)
LACTIC ACID, UNSPECIFIED FORM(UNII: 33X04XA5AT)
HYDROXYPROPYL CELLULOSE (1600000 WAMW)(UNII: RFW2ET671P)
SODIUM LACTATE(UNII: TU7HW0W0QT)
BUTYLATED HYDROXYTOLUENE(UNII: 1P9D0Z171K)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0023-6118-033.5 g in 1 TUBE, WITH APPLICATOR Type 0: Not a Combination Product13/03/1997
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020529 03/13/1997

LABELER - Allergan, Inc.(144796497)

PRINCIPAL DISPLAY PANEL

NDC 0023-6118-03
3.5 g
Condylox ® Gel 0.5%
(podofilox gel)
Allergan™
FOR TOPICAL USE ONLY
Rx only

PRINCIPAL DISPLAY PANEL NDC 0023-6118-03 3.5 g Condylox® Gel 0.5% (podofilox gel) Allergan™ FOR TOPICAL USE ONLY Rx only