Anxiolix Liquid
NDC Package 61657-0006-1

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

Package Information

Anxiolix (arsenicum album , scutellaria lateriflora, phosphorus, lachesis mutus, pulsatilla, passiflora incarnata, aconite, valeriana officinalis, calcarea carbonica, ignatia amara) liquids is iNDICATIONS: FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS. This formulation utilizes a liquid delivery system. Marketed by White Manufacturing Inc. Dba Micro West, this product is identified by NDC 61657-0006.

Identification & Billing

NDC Package Code
61657-0006-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
61657-0006
11-Digit Billing Format
61657000601

Clinical Specifications

Proprietary Name
Anxiolix
Non-Proprietary Name
Arsenicum Album , Scutellaria Lateriflora, Phosphorus, Lachesis Mutus, Pulsatilla, Passiflora Incarnata, Aconite, Valeriana Officinalis, Calcarea Carbonica, Ignatia Amara
Substance Name
Aconitum Napellus; Arsenic Trioxide; Lachesis Muta Venom; Oyster Shell Calcium Carbonate, Crude; Passiflora Incarnata Flowering Top; Phosphorus; Pulsatilla Vulgaris; Scutellaria Lateriflora; Strychnos Ignatii Seed; Valerian
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)
Usage Information
INDICATIONS: FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS

Regulatory & Marketing

Labeler Name
White Manufacturing Inc. Dba Micro West
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-01-2011
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 61657-0006-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Anxiolix, a human over the counter drug labeled by White Manufacturing Inc. Dba Micro West. This liquid is formulated for oral use and contains aconitum napellus; arsenic trioxide; lachesis muta venom; oyster shell calcium carbonate, crude; passiflora incarnata flowering top; phosphorus; pulsatilla vulgaris; scutellaria lateriflora; strychnos ignatii seed; valerian 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 White Manufacturing Inc. Dba Micro West on June 01, 2011. The current certification is valid through December 31, 2026.

How is this White Manufacturing Inc. Dba Micro West product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61657000601. 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)
61657-0006-1
11-Digit CMS (5-4-2)
61657-0006-01

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