Spinalmax Liquid
NDC Package 43742-1326-1

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

Package Information

Spinalmax (berberis vulgaris, cimicifuga racemosa, cinchona officinalis, colocynthis, ledum palustre, ranunculus bulbosus, aesculus hippocastanum, cuprum aceticum, nadidum, natrum oxalaceticum, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, thiaminum hydrochloricum, alpha-lipoicum acidum, ammonium muriaticum, cartilago suis, discus intervertebralis (suis), picricum acidum, silicea, argentum metallicum, calcarea phosphorica, funiculus umbilicalis suis, glandula suprarenalis suis, gnaphalium polycephalum) liquids is for temporary relief of symptoms related to spine issues including spasm, pain, anxiety, nervousness and the inability to hold chiropractic spinal adjustments.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1326.

Identification & Billing

NDC Package Code
43742-1326-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-1326
11-Digit Billing Format
43742132601

Clinical Specifications

Proprietary Name
Spinalmax
Non-Proprietary Name
Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Picricum Acidum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum
Substance Name
Berberis Vulgaris Root Bark; Black Cohosh; Cinchona Officinalis Bark; Citrullus Colocynthis Fruit Pulp; Rhododendron Tomentosum Leafy Twig; Ranunculus Bulbosus; Horse Chestnut; Cupric Acetate; Nadide; Sodium Diethyl Oxalacetate; Niacinamide; Pyridoxine Hydrochloride; Riboflavin; Thiamine Hydrochloride; Alpha Lipoic Acid; Ammonium Chloride; Sus Scrofa Cartilage; Sus Scrofa Intervertebral Disc; Picric Acid; Silicon Dioxide; Silver; Tribasic Calcium Phosphate; Sus Scrofa Umbilical Cord; Sus Scrofa Adrenal Gland; Pseudognaphalium Obtusifolium Whole; Sus Scrofa Bone Marrow; Mercuric Oxide; Pantothenic Acid; Sulfur; Enterobacter Cloacae; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Proteus Morganii; Proteus Vulgaris
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 temporary relief of symptoms related to spine issues including spasm, pain, anxiety, nervousness and the inability to hold chiropractic spinal adjustments.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to spine issues including spasm, pain, anxiety, nervousness and the inability to hold chiropractic spinal adjustments.****These statements are based upon traditional 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
05-17-2019
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 43742-1326-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Spinalmax, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains berberis vulgaris root bark; black cohosh; cinchona officinalis bark; citrullus colocynthis fruit pulp; rhododendron tomentosum leafy twig; ranunculus bulbosus; horse chestnut; cupric acetate; nadide; sodium diethyl oxalacetate; niacinamide; pyridoxine hydrochloride; riboflavin; thiamine hydrochloride; alpha lipoic acid; ammonium chloride; sus scrofa cartilage; sus scrofa intervertebral disc; picric acid; silicon dioxide; silver; tribasic calcium phosphate; sus scrofa umbilical cord; sus scrofa adrenal gland; pseudognaphalium obtusifolium whole; sus scrofa bone marrow; mercuric oxide; pantothenic acid; sulfur; enterobacter cloacae; salmonella enterica subsp. enterica serovar enteritidis; proteus morganii; proteus vulgaris 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 May 17, 2019. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742132601. 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)
43742-1326-1
11-Digit CMS (5-4-2)
43742-1326-01

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