Umecta - 68712-004-02 - (Urea)

Alphabetical Index


Drug Information of Umecta

Product NDC: 68712-004
Proprietary Name: Umecta
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

Product NDC: 68712-004
Labeler Name: Innocutis Holdings LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20040601

Package Information of Umecta

Package NDC: 68712-004-02
Package Description: 3 g in 1 PACKET (68712-004-02)

NDC Information of Umecta

NDC Code 68712-004-02
Proprietary Name Umecta
Package Description 3 g in 1 PACKET (68712-004-02)
Product NDC 68712-004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Urea
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20040601
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


General Information