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  5. NDC Package Code: 63931-4318-1 Wl-aai-zt-p-523

NDC Package 63931-4318-1 Wl-aai-zt-p-523

Titanium Dioxide,Zinc Oxide Powder 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:
63931-4318-1
Package Description:
10000 g in 1 BAG
Product Code:
63931-4318
Proprietary Name:
Wl-aai-zt-p-523
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
11-Digit NDC Billing Format:
63931431801
Product Type:
Human Otc Drug
Labeler Name:
Nanophase Technologies Corporation
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
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):
  • TITANIUM DIOXIDE .125 g/g
  • ZINC OXIDE .225 g/g
    • Sample Package:
    No
    FDA Application Number:
    part352
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    07-15-2019
    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 63931-4318-1?

    The NDC Packaged Code 63931-4318-1 is assigned to a package of 10000 g in 1 bag of Wl-aai-zt-p-523, a human over the counter drug labeled by Nanophase Technologies Corporation. The product's dosage form is powder and is administered via topical form.

    Is NDC 63931-4318 included in the NDC Directory?

    Yes, Wl-aai-zt-p-523 with product code 63931-4318 is active and included in the NDC Directory. The product was first marketed by Nanophase Technologies Corporation on July 15, 2019 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 63931-4318-1?

    The 11-digit format is 63931431801. 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 5-4-1 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
    5-4-163931-4318-15-4-263931-4318-01