NDC Package 59050-456-11 Prep Pad Sterile

Povidone-iodine Patch Topical - View Billable Units, 11-Digit Format, RxNorm

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:
59050-456-11
Package Description:
5.5 g in 1 POUCH
Product Code:
Proprietary Name:
Prep Pad Sterile
Non-Proprietary Name:
Povidone-iodine
Substance Name:
Povidone-iodine
Usage Information:
This product is used as Antiseptic
11-Digit NDC Billing Format:
59050045611
NDC to RxNorm Crosswalk:
  • RxCUI: 1300277 - povidone-iodine gel 10 % Medicated Pad
  • RxCUI: 1300277 - povidone-iodine 0.1 MG/MG Medicated Pad
  • RxCUI: 1300277 - povidone-iodine 10 % (titratable iodine 1 % ) Gel Swabstick
  • RxCUI: 1300277 - povidone-iodine 10 % Gel Swabstick
  • RxCUI: 1300277 - povidone-iodine 10 % Swabstick
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Changzhou Maokang Medical Products Co., Ltd
    Dosage Form:
    Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
    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):
    Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-29-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 59050-456-11?

    The NDC Packaged Code 59050-456-11 is assigned to a package of 5.5 g in 1 pouch of Prep Pad Sterile, a human over the counter drug labeled by Changzhou Maokang Medical Products Co., Ltd. The product's dosage form is patch and is administered via topical form.

    Is NDC 59050-456 included in the NDC Directory?

    Yes, Prep Pad Sterile with product code 59050-456 is active and included in the NDC Directory. The product was first marketed by Changzhou Maokang Medical Products Co., Ltd on June 29, 2018 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 59050-456-11?

    The 11-digit format is 59050045611. 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
    5-3-259050-456-115-4-259050-0456-11