NDC Package 58443-0125-6 Suntone After Sun Burn Relief Gel With Lidocaine

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:
58443-0125-6
Package Description:
470 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Suntone After Sun Burn Relief Gel With Lidocaine
Usage Information:
Adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: Ask a doctor
11-Digit NDC Billing Format:
58443012506
NDC to RxNorm Crosswalk:
  • RxCUI: 1723988 - lidocaine HCl 0.72 % Topical Gel
  • RxCUI: 1723988 - lidocaine hydrochloride 0.0072 MG/MG Topical Gel
  • RxCUI: 1723988 - lidocaine hydrochloride 0.72 % Topical Gel
  • Labeler Name:
    Prime Enterprises Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-07-2011
    Listing Expiration Date:
    12-31-2022
    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 58443-0125-6?

    The NDC Packaged Code 58443-0125-6 is assigned to a package of 470 ml in 1 bottle of Suntone After Sun Burn Relief Gel With Lidocaine, labeled by Prime Enterprises Inc.. The product's dosage form is and is administered via form.

    Is NDC 58443-0125 included in the NDC Directory?

    No, Suntone After Sun Burn Relief Gel With Lidocaine with product code 58443-0125 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Prime Enterprises Inc. on November 07, 2011 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 58443-0125-6?

    The 11-digit format is 58443012506. 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
    5-4-158443-0125-65-4-258443-0125-06