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  5. NDC Package Code: 53329-153-44 Medline

NDC Package 53329-153-44 Medline

White Petrolatum,Zinc Oxide Paste 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:
53329-153-44
Package Description:
113 g in 1 TUBE
Product Code:
53329-153
Proprietary Name:
Medline
Non-Proprietary Name:
White Petrolatum, Zinc Oxide
Substance Name:
White Petrolatum; Zinc Oxide
Usage Information:
For skin protection: apply as needed for diaper rash: change wet and soiled diapers promptly, cleanse the diaper area, and allow to dry apply liberally, as often as necessary, with each diaper change, especially at bedtime or any time when exposure to wet diapers may be prolonged
11-Digit NDC Billing Format:
53329015344
NDC to RxNorm Crosswalk:
  • RxCUI: 1494207 - petrolatum 49 % / zinc oxide 15 % Paste
  • RxCUI: 1494207 - petrolatum 0.49 MG/MG / zinc oxide 0.15 MG/MG Paste
  • RxCUI: 1494207 - Petrolatum 0.49 MG/MG / ZNO 0.15 MG/MG Paste
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Medline Industries, Lp
    Dosage Form:
    Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty 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):
  • WHITE PETROLATUM 490 mg/g
  • ZINC OXIDE 150 mg/g
    • Sample Package:
    No
    FDA Application Number:
    M016
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-01-2023
    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 53329-153-44?

    The NDC Packaged Code 53329-153-44 is assigned to a package of 113 g in 1 tube of Medline, a human over the counter drug labeled by Medline Industries, Lp. The product's dosage form is paste and is administered via topical form.

    Is NDC 53329-153 included in the NDC Directory?

    Yes, Medline with product code 53329-153 is active and included in the NDC Directory. The product was first marketed by Medline Industries, Lp on May 01, 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 53329-153-44?

    The 11-digit format is 53329015344. 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
    5-3-253329-153-445-4-253329-0153-44