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  5. NDC Package Code: 71880-0002-1 Healexir

NDC Package 71880-0002-1 Healexir

Arnica Montana Liquid Oral - 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:
71880-0002-1
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
71880-0002
Proprietary Name:
Healexir
Non-Proprietary Name:
Arnica Montana
Substance Name:
Arnica Montana Whole
Usage Information:
•Spray single pump into mouth at these intervals:•Take every 15 minutes (while awake) for first 48 hours following procedure.•Take every hour (while awake) for the next 48 hours.•Take every 2 hours for the following 5 days.•Take 3 times a day for the next 5 days.•Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
71880000201
Product Type:
Human Otc Drug
Labeler Name:
Healexir, Llc
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):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ARNICA MONTANA WHOLE 1 [hp_M]/mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    08-30-2019
    End Marketing Date:
    03-24-2025
    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 71880-0002-1?

    The NDC Packaged Code 71880-0002-1 is assigned to a package of 30 ml in 1 bottle, spray of Healexir, a human over the counter drug labeled by Healexir, Llc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71880-0002 included in the NDC Directory?

    Yes, Healexir with product code 71880-0002 is active and included in the NDC Directory. The product was first marketed by Healexir, Llc on August 30, 2019.

    What is the 11-digit format for NDC 71880-0002-1?

    The 11-digit format is 71880000201. 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
    5-4-171880-0002-15-4-271880-0002-01