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  5. NDC Package Code: 68712-020-01 Umecta Mousse Urea

NDC Package 68712-020-01 Umecta Mousse Urea

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
68712-020-01
Package Description:
113.4 g in 1 CAN
Product Code:
68712-020
Proprietary Name:
Umecta Mousse Urea
Usage Information:
For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis, keratoderma, corns, and calluses, as well as damaged, ingrown and devitalized nails.
11-Digit NDC Billing Format:
68712002001
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
113.4 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 700903 - urea 40 % Topical Foam
  • RxCUI: 700903 - urea 400 MG/ML Topical Foam
  • RxCUI: 748312 - Umecta 40 % Topical Foam
  • RxCUI: 748312 - urea 400 MG/ML Topical Foam [Umecta]
  • RxCUI: 748312 - Umecta 40 % Topical Mousse
    • Labeler Name:
    Innocutis Holdings Llc
    Sample Package:
    No
    Start Marketing Date:
    09-01-2007
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68712-020-01?

    The NDC Packaged Code 68712-020-01 is assigned to a package of 113.4 g in 1 can of Umecta Mousse Urea, labeled by Innocutis Holdings Llc. The product's dosage form is and is administered via form.This product is billed per "GM" gram and contains an estimated amount of 113.4 billable units per package.

    Is NDC 68712-020 included in the NDC Directory?

    No, Umecta Mousse Urea with product code 68712-020 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Innocutis Holdings Llc on September 01, 2007 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 68712-020-01?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 113.4.

    What is the 11-digit format for NDC 68712-020-01?

    The 11-digit format is 68712002001. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-268712-020-015-4-268712-0020-01