NDC Package 50544-150-44 Acne Wipeout Clinical Acne System

View Billable Units, 11-Digit Format, RxNorm

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:
50544-150-44
Package Description:
1 KIT in 1 KIT * 120 mL in 1 TUBE * 30 mL in 1 TUBE * 60 mL in 1 TUBE
Product Code:
Proprietary Name:
Acne Wipeout Clinical Acne System
Usage Information:
Adults and children 12 years of age and older:Use every morning after cleansing with Acne Wipeout™ Clear Pore Oil-Free Cleanser. Apply a dime-size amount to clean skin, avoiding the eye area. Do not rinse. If bothersome dryness or irritation occurs, reduce frequency of use. Adults and children 12 years of age and older:Use every morning and evening. Apply to damp skin and gently massage, avoiding the eye area. Rinse well. If bothersome dryness or irritation occurs, reduce frequency of use. Use only at night. Apply to face after cleansing with Acne Wipeout™ Clear Pore Oil-Free Cleanser. Do not rinse. Limit sun exposure, and use sunscreen when going outdoors. Formulated to minimize irritation. If any irritation occurs, reduce frequency of use. 
11-Digit NDC Billing Format:
50544015044
NDC to RxNorm Crosswalk:
  • RxCUI: 308693 - benzoyl peroxide 5 % Topical Cream
  • RxCUI: 308693 - benzoyl peroxide 50 MG/ML Topical Cream
  • RxCUI: 845836 - benzoyl peroxide 2.5 % Medicated Liquid Soap
  • RxCUI: 845836 - benzoyl peroxide 25 MG/ML Medicated Liquid Soap
  • Labeler Name:
    University Medical Pharmaceuticals Corp.
    Sample Package:
    No
    Start Marketing Date:
    06-01-2020
    Listing Expiration Date:
    12-31-2022
    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 50544-150-44?

    The NDC Packaged Code 50544-150-44 is assigned to a package of 1 kit in 1 kit * 120 ml in 1 tube * 30 ml in 1 tube * 60 ml in 1 tube of Acne Wipeout Clinical Acne System, labeled by University Medical Pharmaceuticals Corp.. The product's dosage form is and is administered via form.

    Is NDC 50544-150 included in the NDC Directory?

    No, Acne Wipeout Clinical Acne System with product code 50544-150 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by University Medical Pharmaceuticals Corp. on June 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50544-150-44?

    The 11-digit format is 50544015044. 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
    5-3-250544-150-445-4-250544-0150-44