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  5. NDC Package Code: 49348-897-39 Alcohol Prep Pads With Pain Relief

NDC Package 49348-897-39 Alcohol Prep Pads With Pain Relief

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
49348-897-39
Package Description:
80 PACKET in 1 CARTON / 1 SWAB in 1 PACKET
Product Code:
49348-897
Proprietary Name:
Alcohol Prep Pads With Pain Relief
Usage Information:
Prior to Injection - Adults and children 2 years of age or older:Apply to the skin just prior to injection. Benzocaine takes a minute to act. for best results, wait briefly and then make injection.Insect bites, skin irritations, minor burns, sunburn - Adults and children 2 years of age or older:Apply to the affected site not more than 3 to 4 times daily.Children under 2 years of age: Ask a doctor.
11-Digit NDC Billing Format:
49348089739
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
80 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 809206 - benzocaine 60 MG/ML / isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Topical Swab
    • Labeler Name:
    Mckesson
    Sample Package:
    No
    Start Marketing Date:
    02-19-2010
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 49348-897-39?

    The NDC Packaged Code 49348-897-39 is assigned to a package of 80 packet in 1 carton / 1 swab in 1 packet of Alcohol Prep Pads With Pain Relief, labeled by Mckesson. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 80 billable units per package.

    Is NDC 49348-897 included in the NDC Directory?

    No, Alcohol Prep Pads With Pain Relief with product code 49348-897 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Mckesson on February 19, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 49348-897-39?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 80.

    What is the 11-digit format for NDC 49348-897-39?

    The 11-digit format is 49348089739. 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
    5-3-249348-897-395-4-249348-0897-39