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  5. NDC Package Code: 41366-056-01 Foaming Hand

NDC Package 41366-056-01 Foaming Hand

Foaming Hand Soap Liquid Extracorporeal - 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:
41366-056-01
Package Description:
259 mL in 1 BOTTLE
Product Code:
41366-056
Proprietary Name:
Foaming Hand
Non-Proprietary Name:
Foaming Hand Soap
Substance Name:
Cocoyl Methyl Monoethanolamine; Lauramidopropyl Betaine
Usage Information:
APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.
11-Digit NDC Billing Format:
41366005601
Product Type:
Human Otc Drug
Labeler Name:
Zhejiang Meimi Technology Co., Ltd.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Extracorporeal - Administration outside of the body.
    • Active Ingredient(s):
  • COCOYL METHYL MONOETHANOLAMINE 1.2 g/100mL
  • LAURAMIDOPROPYL BETAINE 5 g/100mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    04-18-2022
    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 41366-056-01?

    The NDC Packaged Code 41366-056-01 is assigned to a package of 259 ml in 1 bottle of Foaming Hand, a human over the counter drug labeled by Zhejiang Meimi Technology Co., Ltd.. The product's dosage form is liquid and is administered via extracorporeal form.

    Is NDC 41366-056 included in the NDC Directory?

    Yes, Foaming Hand with product code 41366-056 is active and included in the NDC Directory. The product was first marketed by Zhejiang Meimi Technology Co., Ltd. on April 18, 2022 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 41366-056-01?

    The 11-digit format is 41366005601. 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
    5-3-241366-056-015-4-241366-0056-01