NDC 68712-020

Umecta Mousse Urea

Urea Foam

Umecta Mousse Urea is a Topical Aerosol, Foam in the Human Prescription Drug category. It is labeled and distributed by Innocutis Holdings Llc. The primary component is Urea.

• Product ID: 68712-020_0e33cbf4-abba-49e1-9ade-8c3e4a7358e5
• NDC: 68712-020
• Product Type: Human Prescription Drug
• Proprietary Name: Umecta Mousse Urea
• Generic Name: Urea Foam
• Dosage Form: Aerosol, Foam
• Route of Administration: TOPICAL
• Marketing Start Date: 2007-09-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Innocutis Holdings LLC
• Substance Name: UREA
• Active Ingredient Strength: 400 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68712-020-01

113.4 g in 1 CAN (68712-020-01)

• Marketing Start Date: 2007-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68712-020-01 [68712002001]

Umecta Mousse Urea AEROSOL, FOAM

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2007-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
UREA	400 mg/g

OpenFDA Data

• SPL SET ID: 53f903a2-2b5c-4584-8e91-2c9f41b883ea
• Manufacturer:
  • Innocutis Holdings LLC
• UNII:
  • 8W8T17847W
• RxNorm Concept Unique ID - RxCUI:
  • 700903
  • 748312

NDC Crossover Matching brand name "Umecta Mousse Urea" or generic name "Urea Foam"

NDC	Brand Name	Generic Name
68712-020	Umecta Mousse	Urea Foam
71403-020	Umecta Mousse	Urea Foam