NDC Package 67777-141-31 Dynarex Povidone Iodine Prep Solution

Povidone Iodine Prep Solution Liquid 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:
67777-141-31
Package Description:
48 BOTTLE in 1 CASE / 118 mL in 1 BOTTLE (67777-141-30)
Product Code:
Proprietary Name:
Dynarex Povidone Iodine Prep Solution
Non-Proprietary Name:
Povidone Iodine Prep Solution
Substance Name:
Povidone-iodine
Usage Information:
Clean the area. Apply product to the operative site prior to surgery.
11-Digit NDC Billing Format:
67777014131
NDC to RxNorm Crosswalk:
  • RxCUI: 312564 - povidone-iodine 10 % Topical Solution
  • RxCUI: 312564 - povidone-iodine 100 MG/ML Topical Solution
  • RxCUI: 312564 - povidone-iodine 10 % (titratable iodine 1 % ) Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Dynarex Corporation
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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:
    part333E
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    05-08-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    67777-141-4124 BOTTLE in 1 CASE / 237 mL in 1 BOTTLE (67777-141-40)
    67777-141-5124 BOTTLE in 1 CASE / 473 mL in 1 BOTTLE (67777-141-50)
    67777-141-614 BOTTLE in 1 CASE / 3790 mL in 1 BOTTLE (67777-141-60)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67777-141-31?

    The NDC Packaged Code 67777-141-31 is assigned to a package of 48 bottle in 1 case / 118 ml in 1 bottle (67777-141-30) of Dynarex Povidone Iodine Prep Solution, a human over the counter drug labeled by Dynarex Corporation. The product's dosage form is liquid and is administered via topical form.

    Is NDC 67777-141 included in the NDC Directory?

    Yes, Dynarex Povidone Iodine Prep Solution with product code 67777-141 is active and included in the NDC Directory. The product was first marketed by Dynarex Corporation on May 08, 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 67777-141-31?

    The 11-digit format is 67777014131. 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
    5-3-267777-141-315-4-267777-0141-31