Kids Relief Liquid
NDC Package 71971-9077-8

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Kids Relief (pulsatilla, allium cepa, arsenicum album, nux vomica, euphrasia offinalis, sabadilla, sticta pulmonaria, araila racemosa, cuprum metallicum) liquids is usesThis homeopathic medicine is made from a combination ofingredients traditionally used to help relieve allergy symptoms*:•sneezing                           •nasal congestion•throat and skin irritation    •teary eyes. This formulation utilizes a liquid delivery system. Marketed by Homeolab International (canada) Inc, this product is identified by NDC 71971-9077.

Identification & Billing

NDC Package Code
71971-9077-8
Package Description
1 BOTTLE in 1 CARTON / 25 mL in 1 BOTTLE
Product Code
71971-9077
11-Digit Billing Format
71971907708

Clinical Specifications

Proprietary Name
Kids Relief
Non-Proprietary Name
Pulsatilla, Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Offinalis, Sabadilla, Sticta Pulmonaria, Araila Racemosa, Cuprum Metallicum
Substance Name
Anemone Pulsatilla; Aralia Racemosa Root; Arsenic Trioxide; Copper; Euphrasia Stricta; Lobaria Pulmonaria; Onion; Schoenocaulon Officinale Seed; Strychnos Nux-vomica Seed
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
UsesThis homeopathic medicine is made from a combination ofingredients traditionally used to help relieve allergy symptoms*:•sneezing                           •nasal congestion•throat and skin irritation    •teary eyes

Regulatory & Marketing

Labeler Name
Homeolab International (canada) Inc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-03-2017
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 71971-9077-8 identifies a specific commercial 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. This liquid is formulated for oral use and contains anemone pulsatilla; aralia racemosa root; arsenic trioxide; copper; euphrasia stricta; lobaria pulmonaria; onion; schoenocaulon officinale seed; strychnos nux-vomica seed as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Homeolab International (canada) Inc on March 03, 2017. The current certification is valid through December 31, 2026.

How is this Homeolab International (canada) Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71971907708. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
71971-9077-8
11-Digit CMS (5-4-2)
71971-9077-08

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.