Umecta PD - 68712-017-02 - (Urea)

Alphabetical Index


Drug Information of Umecta PD

Product NDC: 68712-017
Proprietary Name: Umecta PD
Non Proprietary Name: Urea
Active Ingredient(s): 400    mg/g & nbsp;   Urea
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Umecta PD

Product NDC: 68712-017
Labeler Name: Innocutis Holdings LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070601

Package Information of Umecta PD

Package NDC: 68712-017-02
Package Description: 198.5 g in 1 BOTTLE (68712-017-02)

NDC Information of Umecta PD

NDC Code 68712-017-02
Proprietary Name Umecta PD
Package Description 198.5 g in 1 BOTTLE (68712-017-02)
Product NDC 68712-017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Urea
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20070601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Innocutis Holdings LLC
Substance Name UREA
Strength Number 400
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Umecta PD


General Information