NDC Package 71971-9066-8 Kids Relief

Pulsatilla,Allium Cepa,Arsenicum Album,Nux Vomica,Euphrasia Offinalis,Sabadilla,Aralia - 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:
71971-9066-8
Package Description:
1 BOTTLE in 1 CARTON / 25 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Kids Relief
Non-Proprietary Name:
Pulsatilla, Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Offinalis, Sabadilla, Aralia Racemosa, Cuprum Metallicum
Substance Name:
Anemone Pulsatilla; Aralia Racemosa Root; Arsenic Trioxide; Copper; Euphrasia Stricta; Onion; Schoenocaulon Officinale Seed; Strychnos Nux-vomica Seed
Usage Information:
UsesThis homeopathic medicine is made from a combination of ingredients traditionally used to help relieve indispositions caused by sinus symptoms*:• sneezing• nasal congestion• runny nose• itchy eyes, nose and throat• watery eyes• headache• throat irritation
11-Digit NDC Billing Format:
71971906608
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:
    07-26-2019
    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 71971-9066-8?

    The NDC Packaged Code 71971-9066-8 is assigned to a package of 1 bottle in 1 carton / 25 ml in 1 bottle of Kids 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 71971-9066 included in the NDC Directory?

    Yes, Kids Relief with product code 71971-9066 is active and included in the NDC Directory. The product was first marketed by Homeolab International (canada) Inc on July 26, 2019 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 71971-9066-8?

    The 11-digit format is 71971906608. 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
    5-4-171971-9066-85-4-271971-9066-08