Real Relief Tablet
NDC Package 71971-6030-5

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

Package Information

Real Relief (allium cepa, aralia racemosa, arsenicum album, cuprum metallicum, euphrasia officinalis, nux vomica, sabadilla, sticta pulmonaria) tablets is usesThis homeopathic remedy to relieve from symptoms of all allergiesNasal congestionSneezingRunny noseItchy, watery eyes. This formulation utilizes a tablet delivery system. Marketed by Homeolab International (canada) Inc, this product is identified by NDC 71971-6030.

Identification & Billing

NDC Package Code
71971-6030-5
Package Description
30 TABLET in 1 BOTTLE
Product Code
71971-6030
11-Digit Billing Format
71971603005

Clinical Specifications

Proprietary Name
Real Relief
Non-Proprietary Name
Allium Cepa, Aralia Racemosa, Arsenicum Album, Cuprum Metallicum, Euphrasia Officinalis, Nux Vomica, Sabadilla, Sticta Pulmonaria
Substance Name
Aralia Racemosa Root; Arsenic Trioxide; Copper; Euphrasia Stricta; Lobaria Pulmonaria; Onion; Schoenocaulon Officinale Seed; Strychnos Nux-vomica Seed
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
UsesThis homeopathic remedy to relieve from symptoms of all allergiesNasal congestionSneezingRunny noseItchy, watery 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
01-01-2020
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 (71971-6030). Click a package code to view its specific billing and regulatory data.

71971-6030-0
1 BOTTLE in 1 CARTON / 90 TABLET in 1 BOTTLE
71971-6030-8
1 BOTTLE in 1 CARTON / 60 TABLET 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 71971-6030-5 identifies a specific commercial package of 30 tablet in 1 bottle of Real Relief, a human over the counter drug labeled by Homeolab International (canada) Inc. This tablet is formulated for oral use and contains 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 January 01, 2020. 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: 71971603005. 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)
71971-6030-5
11-Digit CMS (5-4-2)
71971-6030-05

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