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  5. NDC Package Code: 53807-123-45 Anti-fungal

NDC Package 53807-123-45 Anti-fungal

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:
53807-123-45
Package Description:
45 g in 1 BOTTLE, DISPENSING
Product Code:
53807-123
Proprietary Name:
Anti-fungal
Usage Information:
Shake well before useclean the affected area and dry thoroughlyapply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productthis product is not effective on the scalp or nails For athletes footuse daily for 4 weeks pay special attention to the spaces between the toeswear well-fitting, ventilated shoeschange shoes and socks at least once a dailyto prevent athlete's foot: clean and dry feet thoroughly, apply once or twice dailyFor jock itchuse daily for 2 weeks
11-Digit NDC Billing Format:
53807012345
NDC to RxNorm Crosswalk:
  • RxCUI: 313422 - tolnaftate 1 % Topical Powder
  • RxCUI: 313422 - tolnaftate 0.01 MG/MG Topical Powder
    • Labeler Name:
    Rij Pharmaceutical Corporation
    Sample Package:
    No
    Start Marketing Date:
    03-16-1999
    Listing Expiration Date:
    12-31-2019
    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 53807-123-45?

    The NDC Packaged Code 53807-123-45 is assigned to a package of 45 g in 1 bottle, dispensing of Anti-fungal, labeled by Rij Pharmaceutical Corporation. The product's dosage form is and is administered via form.

    Is NDC 53807-123 included in the NDC Directory?

    No, Anti-fungal with product code 53807-123 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rij Pharmaceutical Corporation on March 16, 1999 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 53807-123-45?

    The 11-digit format is 53807012345. 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
    5-3-253807-123-455-4-253807-0123-45