Bio Tonsilla Phase Liquid
NDC Package 43742-1600-1

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

Package Information

Bio Tonsilla Phase (dulcamara, echinacea (angustifolia), aesculus hippocastanum, antimonium tartaricum, ascorbicum acidum, coccus cacti, galium aparine, gentiana lutea, geranium robertianum, pulsatilla (pratensis), sarcolacticum acidum, acetylcholine chloride, mannose, conium maculatum, lymph node (suis), sulphur, calcarea phosphorica, funiculus umbilicalis suis, hepar suis, hypothalamus suis, medulla ossis suis, spleen (suis), cortisone aceticum, glandula suprarenalis suis, mercurius solubilis, thyroidinum (suis),) liquids is for the temporary relief of symptoms such as sore throat, pain, swelling, and inflammation.****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 43742-1600.

Identification & Billing

NDC Package Code
43742-1600-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-1600
11-Digit Billing Format
43742160001

Clinical Specifications

Proprietary Name
Bio Tonsilla Phase
Non-Proprietary Name
Dulcamara, Echinacea (angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (pratensis), Sarcolacticum Acidum, Acetylcholine Chloride, Mannose, Conium Maculatum, Lymph Node (suis), Sulphur, Calcarea Phosphorica, Funiculus Umbilicalis Suis, Hepar Suis, Hypothalamus Suis, Medulla Ossis Suis, Spleen (suis), Cortisone Aceticum, Glandula Suprarenalis Suis, Mercurius Solubilis, Thyroidinum (suis),
Substance Name
Solanum Dulcamara Top; Echinacea Angustifolia Whole; Horse Chestnut; Antimony Potassium Tartrate; Ascorbic Acid; Protortonia Cacti; Galium Aparine Whole; Gentiana Lutea Root; Geranium Robertianum Whole; Pulsatilla Pratensis Whole; Lactic Acid, L-; Acetylcholine Chloride; Mannose, D-; Conium Maculatum Flowering Top; Sus Scrofa Lymph; Sulfur; Tribasic Calcium Phosphate; Sus Scrofa Umbilical Cord; Pork Liver; Sus Scrofa Hypothalamus; Sus Scrofa Bone Marrow; Sus Scrofa Spleen; Cortisone Acetate; Sus Scrofa Adrenal Gland; Mercurius Solubilis; Sus Scrofa Thyroid; Barium Carbonate; Sus Scrofa Tonsil
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 sore throat, pain, swelling, and inflammation.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician. For the temporary relief of symptoms such as sore throat, pain, swelling, and inflammation.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.

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
10-29-2019
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 43742-1600-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Bio Tonsilla Phase, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains solanum dulcamara top; echinacea angustifolia whole; horse chestnut; antimony potassium tartrate; ascorbic acid; protortonia cacti; galium aparine whole; gentiana lutea root; geranium robertianum whole; pulsatilla pratensis whole; lactic acid, l-; acetylcholine chloride; mannose, d-; conium maculatum flowering top; sus scrofa lymph; sulfur; tribasic calcium phosphate; sus scrofa umbilical cord; pork liver; sus scrofa hypothalamus; sus scrofa bone marrow; sus scrofa spleen; cortisone acetate; sus scrofa adrenal gland; mercurius solubilis; sus scrofa thyroid; barium carbonate; sus scrofa tonsil 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 October 29, 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: 43742160001. 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)
43742-1600-1
11-Digit CMS (5-4-2)
43742-1600-01

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