Spectric Liquid
NDC Package 43742-2066-1

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

Package Information

Spectric (ethylicum, kali bromatum, aspartame, l-dopa, serotonin (hydrochloride), cerebrum suis, placenta totalis suis, agaricus muscarius, bufo rana, helleborus niger, hyoscyamus niger, olibanum (boswellia serrata), stramonium, thuja occidentalis, helium, neon, carcinosin, hydrogen) liquids is for the temporary relief of symptoms such as agitation, lack of empathy, angry outburst, repetitive behaviors, repetitive speech, delayed language development, indifferent to human interaction, and precocity.****These statements are based upon homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc, this product is identified by NDC 43742-2066.

Identification & Billing

NDC Package Code
43742-2066-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-2066
11-Digit Billing Format
43742206601

Clinical Specifications

Proprietary Name
Spectric
Non-Proprietary Name
Ethylicum, Kali Bromatum, Aspartame, L-dopa, Serotonin (hydrochloride), Cerebrum Suis, Placenta Totalis Suis, Agaricus Muscarius, Bufo Rana, Helleborus Niger, Hyoscyamus Niger, Olibanum (boswellia Serrata), Stramonium, Thuja Occidentalis, Helium, Neon, Carcinosin, Hydrogen
Substance Name
Alcohol; Amanita Muscaria Whole; Aspartame; Bufo Bufo Cutaneous Gland; Datura Stramonium; Helium; Helleborus Niger Root; Human Breast Tumor Cell; Hydrogen; Hyoscyamus Niger; Indian Frankincense; Levodopa; Neon; Potassium Bromide; Serotonin Hydrochloride; Sus Scrofa Cerebrum; Sus Scrofa Placenta; Thuja Occidentalis Leafy Twig
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)
Pharmacologic Class
Usage Information
For the temporary relief of symptoms such as agitation, lack of empathy, angry outburst, repetitive behaviors, repetitive speech, delayed language development, indifferent to human interaction, and precocity.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms such as agitation, lack of empathy, angry outburst, repetitive behaviors, repetitive speech, delayed language development, indifferent to human interaction, and precocity.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Deseret Biologicals, 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
11-08-2022
End Marketing Date
12-28-2028
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 43742-2066-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Spectric, a human over the counter drug labeled by Deseret Biologicals, Inc. This liquid is formulated for oral use and contains alcohol; amanita muscaria whole; aspartame; bufo bufo cutaneous gland; datura stramonium; helium; helleborus niger root; human breast tumor cell; hydrogen; hyoscyamus niger; indian frankincense; levodopa; neon; potassium bromide; serotonin hydrochloride; sus scrofa cerebrum; sus scrofa placenta; thuja occidentalis leafy twig 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 Deseret Biologicals, Inc on November 08, 2022.

How is this Deseret Biologicals, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742206601. 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)
43742-2066-1
11-Digit CMS (5-4-2)
43742-2066-01

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