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  5. NDC Package Code: 82081-0001-1 Nwk A-fv

NDC Package 82081-0001-1 Nwk A-fv

Cochlearia Armoracia(horseradish) Root Extract Liquid 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:
82081-0001-1
Package Description:
20000 mL in 1 BOTTLE
Product Code:
82081-0001
Proprietary Name:
Nwk A-fv
Non-Proprietary Name:
Cochlearia Armoracia(horseradish) Root Extract
Substance Name:
Horseradish
Usage Information:
Apply where needed
11-Digit NDC Billing Format:
82081000101
Product Type:
Human Otc Drug
Labeler Name:
Nae Woi Korea 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):
  • 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):
  • HORSERADISH 10 g/100mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Food Additives - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
    • 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:
    07-14-2021
    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 82081-0001-1?

    The NDC Packaged Code 82081-0001-1 is assigned to a package of 20000 ml in 1 bottle of Nwk A-fv, a human over the counter drug labeled by Nae Woi Korea Ltd. The product's dosage form is liquid and is administered via topical form.

    Is NDC 82081-0001 included in the NDC Directory?

    Yes, Nwk A-fv with product code 82081-0001 is active and included in the NDC Directory. The product was first marketed by Nae Woi Korea Ltd on July 14, 2021 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 82081-0001-1?

    The 11-digit format is 82081000101. 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 5-4-1 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
    5-4-182081-0001-15-4-282081-0001-01