Kids Relief Liquid
NDC Package 71971-9151-4

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Kids Relief (drosera, arnica montana, bryonia, cetraria islandica, coccus cacti, corallium rubrum, stannum metallicum, chamomilla, coffee crudea) liquids is part 1 Kids Relief Daytime SyrupChildren under 6 months of age: consult a licensed healthcare practitioner before using the product. This formulation utilizes a liquid delivery system. Marketed by Homeolab International (canada) Inc, this product is identified by NDC 71971-9151.

Identification & Billing

NDC Package Code
71971-9151-4
Package Description
30 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
71971915104

Clinical Specifications

Proprietary Name
Kids Relief
Non-Proprietary Name
Drosera, Arnica Montana, Bryonia, Cetraria Islandica, Coccus Cacti, Corallium Rubrum, Stannum Metallicum, Chamomilla, Coffee Crudea
Substance Name
Arabica Coffee Bean; Arnica Montana; Bryonia Alba Whole; Cetraria Islandica Subsp. Islandica; Chamomile; Corallium Rubrum Whole; Drosera Rotundifolia Flowering Top; Protortonia Cacti; Tin
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.
Usage Information
Part 1 Kids Relief Daytime SyrupChildren under 6 months of age: consult a licensed healthcare practitioner before using the product. Children 6 months to 2 years old: 2.5 ml or ½ teaspoon, every 6 hours or 4 times a day. Children 2 to 12 years old: 5 ml or 1 teaspoon, every 6 hours or 4 times a day.Part 2 Kids Relief Nighttime SyrupChildren under 6 months of age: consult a licensed healthcare practitioner before using the product. Children 6 months to 2 years old: 2.5 ml or ½ teaspoon, every 8 hours or 3 times a day. Children 2 to 12 years old: 5 ml or 1 teaspoon, every 8 hours or 3 times a day.

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
03-03-2018
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71971-9151). Click a package code to view its specific billing and regulatory data.

1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE
1 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE

* 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 71971-9151-4 identifies a specific commercial package of 30 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 arabica coffee bean; arnica montana; bryonia alba whole; cetraria islandica subsp. islandica; chamomile; corallium rubrum whole; drosera rotundifolia flowering top; protortonia cacti; tin 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, 2018. 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: 71971915104. 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)
71971-9151-4
11-Digit CMS (5-4-2)
71971-9151-04

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