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  5. NDC Package Code: 41190-083-01 Shoprite

NDC Package 41190-083-01 Shoprite

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:
41190-083-01
Package Description:
1 TUBE in 1 CARTON / 15 g in 1 TUBE
Product Code:
41190-083
Proprietary Name:
Shoprite
Usage Information:
Adults and children 12 years and olderuse the tip of the cap to break the seal and open the tubewash the affected skin with soap and water and dry completely before applyingfor athlete's foot wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.between the toes only: apply twice a day (morning and night) for 1 week or as directed by a doctor.on the bottom or sides of the foot: apply twice a day (morning and night) for 2 weeks or as directed by a doctor.for jock itch and ringworm: apply once a day (morning or night) for 1 week or as directed by a doctor.wash hands after each usechildren under 12 years: ask a doctor1 weekbetween the toes2 weeks on the bottomor sides of the foot
11-Digit NDC Billing Format:
41190008301
NDC to RxNorm Crosswalk:
  • RxCUI: 992528 - terbinafine HCl 1 % Topical Cream
  • RxCUI: 992528 - terbinafine hydrochloride 10 MG/ML Topical Cream
  • RxCUI: 992528 - terbinafine hydrochloride 1 % Topical Cream
    • Labeler Name:
    Wakefern Food Corporation
    Sample Package:
    No
    Start Marketing Date:
    07-02-2007
    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 41190-083-01?

    The NDC Packaged Code 41190-083-01 is assigned to a package of 1 tube in 1 carton / 15 g in 1 tube of Shoprite, labeled by Wakefern Food Corporation. The product's dosage form is and is administered via form.

    Is NDC 41190-083 included in the NDC Directory?

    No, Shoprite with product code 41190-083 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Wakefern Food Corporation on July 02, 2007 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 41190-083-01?

    The 11-digit format is 41190008301. 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
    5-3-241190-083-015-4-241190-0083-01