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  5. NDC Package Code: 61333-202-01 Lights Povidone Iodine Solution

NDC Package 61333-202-01 Lights Povidone Iodine Solution

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

Table of Contents

    1. Package Information
    2. 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:
61333-202-01
Package Description:
118 mL in 1 BOTTLE
Product Code:
61333-202
Proprietary Name:
Lights Povidone Iodine Solution
Non-Proprietary Name:
Povidone-iodine
Substance Name:
Povidone-iodine
Usage Information:
Use: Antiseptic skin preparation
11-Digit NDC Billing Format:
61333020201
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:
    Lights Medical Manufacture Co., Ltd.
    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 1.18 g/118mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-22-2014
    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.

    Frequently Asked Questions

    What is NDC 61333-202-01?

    The NDC Packaged Code 61333-202-01 is assigned to a package of 118 ml in 1 bottle of Lights Povidone Iodine Solution, a human over the counter drug labeled by Lights Medical Manufacture Co., Ltd.. The product's dosage form is solution and is administered via topical form.

    Is NDC 61333-202 included in the NDC Directory?

    Yes, Lights Povidone Iodine Solution with product code 61333-202 is active and included in the NDC Directory. The product was first marketed by Lights Medical Manufacture Co., Ltd. on March 22, 2014 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 61333-202-01?

    The 11-digit format is 61333020201. 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
    5-3-261333-202-015-4-261333-0202-01