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  5. NDC Package Code: 83254-705-25 Povidone Iodine

NDC Package 83254-705-25 Povidone Iodine

Povidone Iodine 7.5 Solution Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
83254-705-25
Package Description:
225 mL in 1 BOTTLE
Product Code:
83254-705
Proprietary Name:
Povidone Iodine
Non-Proprietary Name:
Povidone Iodine 7.5 Solution
Substance Name:
Povidone-iodine
Usage Information:
Apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks. If the condition persists longer, consult a doctor. This product is not effective on the scalp or nails.To prevent athlete's foot, wash the feet and dry thoroughly. Apply a thin layer of the product to the feet once or twice daily (morning and/or night). Supervise children in the use of this product. Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
11-Digit NDC Billing Format:
83254070525
NDC to RxNorm Crosswalk:
  • RxCUI: 1546212 - povidone-iodine 0.75 % Topical Solution
  • RxCUI: 1546212 - povidone-iodine 7.5 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    1201258 Ontario Inc. O/a Nanz Pharma
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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):
  • POVIDONE-IODINE 7.5 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    05-04-2023
    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
    83254-705-01100 mL in 1 BOTTLE
    83254-705-02200 mL in 1 BOTTLE
    83254-705-05500 mL in 1 BOTTLE
    83254-705-101000 mL in 1 BOTTLE
    83254-705-1130 mL in 1 POUCH
    83254-705-15150 mL in 1 BOTTLE
    83254-705-18118 mL in 1 BOTTLE
    83254-705-20120 mL in 1 BOTTLE
    83254-705-2260 mL in 1 POUCH
    83254-705-3390 mL in 1 POUCH
    83254-705-5050 mL in 1 BOTTLE
    83254-705-6060 mL in 1 BOTTLE
    83254-705-9090 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 83254-705-25?

    The NDC Packaged Code 83254-705-25 is assigned to a package of 225 ml in 1 bottle of Povidone Iodine, a human over the counter drug labeled by 1201258 Ontario Inc. O/a Nanz Pharma. The product's dosage form is solution and is administered via topical form.

    Is NDC 83254-705 included in the NDC Directory?

    Yes, Povidone Iodine with product code 83254-705 is active and included in the NDC Directory. The product was first marketed by 1201258 Ontario Inc. O/a Nanz Pharma on May 04, 2023 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 83254-705-25?

    The 11-digit format is 83254070525. 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
    5-3-283254-705-255-4-283254-0705-25