Anxiety Relief Tablet
NDC Package 70163-0047-2

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

Package Information

Anxiety Relief (aconitum napellus, argentum nitricum, arsenicum album, aurum metallicum, gelsemium sempervirens, hyoscyamus niger, ignatia amara, kali carbonicum, moschus, natrum muriaticum, piper methysticum) tablets is adults and children over the age of 12: ■ dissolve 1-2 tablets under the tongue 3 times daily. This formulation utilizes a tablet delivery system. Marketed by Naturalcare, this product is identified by NDC 70163-0047.

Identification & Billing

NDC Package Code
70163-0047-2
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 120 TABLET in 1 BOTTLE, PLASTIC (70163-0047-1)
Product Code
70163-0047
11-Digit Billing Format
70163004702

Clinical Specifications

Proprietary Name
Anxiety Relief
Non-Proprietary Name
Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Aurum Metallicum, Gelsemium Sempervirens, Hyoscyamus Niger, Ignatia Amara, Kali Carbonicum, Moschus, Natrum Muriaticum, Piper Methysticum
Substance Name
Aconitum Napellus Whole; Arsenic Trioxide; Gelsemium Sempervirens Root; Gold; Hyoscyamus Niger; Moschus Moschiferus Musk Sac Resin; Piper Methysticum Root; Potassium Carbonate; Silver Nitrate; Sodium Chloride; Strychnos Ignatii 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
Adults and children over the age of 12: ■ dissolve 1-2 tablets under the tongue 3 times daily.

Regulatory & Marketing

Labeler Name
Naturalcare
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-15-2026
Listing Expiration
12-31-2027
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 70163-0047-2 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 120 tablet in 1 bottle, plastic (70163-0047-1) of Anxiety Relief, a human over the counter drug labeled by Naturalcare. This tablet is formulated for oral use and contains aconitum napellus whole; arsenic trioxide; gelsemium sempervirens root; gold; hyoscyamus niger; moschus moschiferus musk sac resin; piper methysticum root; potassium carbonate; silver nitrate; sodium chloride; strychnos ignatii 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 Naturalcare on April 15, 2026. The current certification is valid through December 31, 2027.

How is this Naturalcare product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70163004702. 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)
70163-0047-2
11-Digit CMS (5-4-2)
70163-0047-02

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