NDC Package 17271-503-01 Bd E-z Scrub

Povidone-iodine Solution 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:
17271-503-01
Package Description:
6 BOTTLE in 1 BOX / 946 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Bd E-z Scrub
Non-Proprietary Name:
Povidone-iodine
Substance Name:
Povidone-iodine
Usage Information:
Surgical Hand ScrubWet hands and forearms with warm water Use nail cleaner and then apply solution from the sponge side to work up a lather Scrub thoroughly for 3 minutes: difficult areas (interdigital space and fingers) with brush side, hands and forarms with sponge side Rinse thoroughly with warm water Repeat scrub for 3 minutes, sponge side only Rinse hands and arms thoroughly Dry thoroughly Health Care Personnel HandwashDispense about 5 ml of foam solution into cupped hands Wash in a vigorous manner covering all surfaces for 30 seconds Rinse thoroughly with running water (30 seconds)
11-Digit NDC Billing Format:
17271050301
Product Type:
Human Otc Drug
Labeler Name:
Becton Dickinson And Company
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):
    Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-01-2000
    End Marketing Date:
    01-31-2025
    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.

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    Frequently Asked Questions

    What is NDC 17271-503-01?

    The NDC Packaged Code 17271-503-01 is assigned to a package of 6 bottle in 1 box / 946 ml in 1 bottle of Bd E-z Scrub, a human over the counter drug labeled by Becton Dickinson And Company. The product's dosage form is solution and is administered via topical form.

    Is NDC 17271-503 included in the NDC Directory?

    Yes, Bd E-z Scrub with product code 17271-503 is active and included in the NDC Directory. The product was first marketed by Becton Dickinson And Company on April 01, 2000.

    What is the 11-digit format for NDC 17271-503-01?

    The 11-digit format is 17271050301. 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
    5-3-217271-503-015-4-217271-0503-01