NDC Package 58988-1600-2 Sanafitil Crema

View Billable Units, 11-Digit Format, RxNorm

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:
58988-1600-2
Package Description:
1 TUBE in 1 BOX / 28.35 g in 1 TUBE
Product Code:
Proprietary Name:
Sanafitil Crema
Usage Information:
Wash affected area and dry thoroughlyapply a thin layer over affected area twice daily (morning and night)supervise children in the use of this productfor athlete's foot, pay special attention to spaces between the toes, wear well-fitting ventilated shoes and change shoes and socks at least once dailyuse daily for 4 weeks; if condition persists longer, ask a doctorto prevent athlete's foot, apply once or twice daily (morning and/or night)this product is not effective on the scalp or nails
11-Digit NDC Billing Format:
58988160002
NDC to RxNorm Crosswalk:
  • RxCUI: 103951 - tolnaftate 1 % Topical Cream
  • RxCUI: 103951 - tolnaftate 10 MG/ML Topical Cream
  • RxCUI: 1599125 - SANAFITIL 1 % Topical Cream
  • RxCUI: 1599125 - tolnaftate 10 MG/ML Topical Cream [Sanafitil Cream]
  • RxCUI: 1599125 - Sanafitil 1 % Topical Cream
  • Labeler Name:
    Promex Llc
    Sample Package:
    No
    Start Marketing Date:
    01-07-2015
    Listing Expiration Date:
    12-31-2017
    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 58988-1600-2?

    The NDC Packaged Code 58988-1600-2 is assigned to a package of 1 tube in 1 box / 28.35 g in 1 tube of Sanafitil Crema, labeled by Promex Llc. The product's dosage form is and is administered via form.

    Is NDC 58988-1600 included in the NDC Directory?

    No, Sanafitil Crema with product code 58988-1600 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Promex Llc on January 07, 2015 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 58988-1600-2?

    The 11-digit format is 58988160002. 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
    5-4-158988-1600-25-4-258988-1600-02