Label: TRIDESILON CREAM- desonide 0.05% cream
- NDC Code(s): 69482-600-60
- Packager: Encore Dermatology Inc
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated April 21, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DESCRIPTION SECTION
- INSTRUCTIONS FOR USE SECTION
- STORAGE AND HANDLING SECTION
- Dosage & Administration Section
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TRIDESILON CREAM
desonide 0.05% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69482-600 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DESONIDE (UNII: J280872D1O) (DESONIDE - UNII:J280872D1O) DESONIDE 0.03 g in 60 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69482-600-60 1 in 1 CARTON 10/01/2016 1 1 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA017010 10/01/2016 Labeler - Encore Dermatology Inc (079629654) Establishment Name Address ID/FEI Business Operations Perrigo New York, Inc 078846912 manufacture(69482-600)
