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  5. NDC Package Code: 50157-333-45 Zinc Oxide

NDC Package 50157-333-45 Zinc Oxide

Ointment Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
50157-333-45
Package Description:
454 g in 1 TUBE
Product Code:
50157-333
Proprietary Name:
Zinc Oxide
Non-Proprietary Name:
Zinc Oxide
Substance Name:
Zinc Oxide
Usage Information:
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.
11-Digit NDC Billing Format:
50157033345
NDC to RxNorm Crosswalk:
  • RxCUI: 198911 - zinc oxide 20 % Topical Ointment
  • RxCUI: 198911 - zinc oxide 0.2 MG/MG Topical Ointment
  • RxCUI: 198911 - zinc oxide 200 MG per GM Topical Ointment
  • RxCUI: 198911 - ZNO 0.2 MG/MG Topical Ointment
    • Product Type:
    Human Otc Drug
    Labeler Name:
    �brands International
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • ZINC OXIDE 20 g/100g
    • Sample Package:
    No
    FDA Application Number:
    part347
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    03-15-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 50157-333-45?

    The NDC Packaged Code 50157-333-45 is assigned to a package of 454 g in 1 tube of Zinc Oxide, a human over the counter drug labeled by �brands International. The product's dosage form is ointment and is administered via topical form.

    Is NDC 50157-333 included in the NDC Directory?

    Yes, Zinc Oxide with product code 50157-333 is active and included in the NDC Directory. The product was first marketed by �brands International on March 15, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50157-333-45?

    The 11-digit format is 50157033345. 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
    5-3-250157-333-455-4-250157-0333-45