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  5. NDC Package Code: 71310-009-01 Lightning X Alcohol Prep Pads

NDC Package 71310-009-01 Lightning X Alcohol Prep Pads

Isopropyl Alcohol Patch 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:
71310-009-01
Package Description:
.4 g in 1 PACKAGE
Product Code:
71310-009
Proprietary Name:
Lightning X Alcohol Prep Pads
Non-Proprietary Name:
Isopropyl Alcohol
Substance Name:
Isopropyl Alcohol
11-Digit NDC Billing Format:
71310000901
NDC to RxNorm Crosswalk:
  • RxCUI: 797544 - isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 797544 - isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 797544 - isopropyl alcohol 70 % Topical Cloth
  • RxCUI: 797544 - isopropyl alcohol 70 % Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Taizhou Kangping Medical Science And Technology Co., Ltd.
    Dosage Form:
    Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
    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):
  • ISOPROPYL ALCOHOL 70 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-08-2024
    Listing Expiration Date:
    12-31-2025
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71310-009-01?

    The NDC Packaged Code 71310-009-01 is assigned to a package of .4 g in 1 package of Lightning X Alcohol Prep Pads, a human over the counter drug labeled by Taizhou Kangping Medical Science And Technology Co., Ltd.. The product's dosage form is patch and is administered via topical form.

    Is NDC 71310-009 included in the NDC Directory?

    Yes, Lightning X Alcohol Prep Pads with product code 71310-009 is active and included in the NDC Directory. The product was first marketed by Taizhou Kangping Medical Science And Technology Co., Ltd. on January 08, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71310-009-01?

    The 11-digit format is 71310000901. 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
    5-3-271310-009-015-4-271310-0009-01