NDC Package 71971-9899-9 Real Relief

Drosera,Arnica Montana,Bryonia,Ipecacuanha,Cetraria Islandica,Coccus Cacti,Corallium - View Billable Units, 11-Digit Format, RxNorm

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:
71971-9899-9
Package Description:
1 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Real Relief
Non-Proprietary Name:
Drosera, Arnica Montana, Bryonia, Ipecacuanha, Cetraria Islandica, Coccus Cacti, Corallium Rubrum, Stannum Metallicum, Camomilla, Coffea Crudea
Substance Name:
Arabica Coffee Bean; Arnica Montana; Bryonia Alba Whole; Cetraria Islandica Subsp. Islandica; Chamomile; Corallium Rubrum Whole; Drosera Rotundifolia Flowering Top; Ipecac; Protortonia Cacti; Tin
Usage Information:
Uses  This homeopathic medicine is made from a combinationof ingredients traditionally used to help relievesymptoms associated with nighttime cough and cold*:•dry cough  •cough with expectoration•chest congestion  •fever  •aches and pains
11-Digit NDC Billing Format:
71971989909
Product Type:
Human Otc Drug
Labeler Name:
Homeolab International (canada) Inc
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.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-03-2018
    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 71971-9899-9?

    The NDC Packaged Code 71971-9899-9 is assigned to a package of 1 bottle in 1 carton / 250 ml in 1 bottle of Real Relief, a human over the counter drug labeled by Homeolab International (canada) Inc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71971-9899 included in the NDC Directory?

    Yes, Real Relief with product code 71971-9899 is active and included in the NDC Directory. The product was first marketed by Homeolab International (canada) Inc on May 03, 2018 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 71971-9899-9?

    The 11-digit format is 71971989909. 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
    5-4-171971-9899-95-4-271971-9899-09