Nativeremedies Backache Ease Tablet
NDC Package 68703-373-80

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

Package Information

Nativeremedies Backache Ease (arnica, bryonia, cimicifuga, hypericum, ignatia, kali carb, nux vom, rhus tox, ruta) tablets is directions: chew or dissolve tablets in the mouth. This formulation utilizes a tablet delivery system. Marketed by Silver Star Brands, this product is identified by NDC 68703-373.

Identification & Billing

NDC Package Code
68703-373-80
Package Description
180 TABLET in 1 BOTTLE, GLASS
Product Code
68703-373
11-Digit Billing Format
68703037380

Clinical Specifications

Proprietary Name
Nativeremedies Backache Ease
Non-Proprietary Name
Arnica, Bryonia, Cimicifuga, Hypericum, Ignatia, Kali Carb, Nux Vom, Rhus Tox, Ruta
Substance Name
Actaea Cimicifuga Root; Arnica Angustifolia Flower; Bryonia Alba Root; Hypericum Perforatum; Potassium Carbonate; Ruta Graveolens Flowering Top; Strychnos Ignatii Seed; Strychnos Nux-vomica Seed; Toxicodendron Radicans Leaf
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
Directions: chew or dissolve tablets in the mouth. For Adults and Children 12+: Take 2 tablets every 15-20 minutes up to 4 doses, then every 4 hours until symptoms subside.

Regulatory & Marketing

Labeler Name
Silver Star Brands
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
09-07-2021
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 68703-373-80 identifies a specific commercial package of 180 tablet in 1 bottle, glass of Nativeremedies Backache Ease, a human over the counter drug labeled by Silver Star Brands. This tablet is formulated for oral use and contains actaea cimicifuga root; arnica angustifolia flower; bryonia alba root; hypericum perforatum; potassium carbonate; ruta graveolens flowering top; strychnos ignatii seed; strychnos nux-vomica seed; toxicodendron radicans leaf 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 Silver Star Brands on September 07, 2021. The current certification is valid through December 31, 2026.

How is this Silver Star Brands product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68703037380. 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 (5-3-2)
68703-373-80
11-Digit CMS (5-4-2)
68703-0373-80

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