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),

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1600

Bio Tonsilla Phase also known as 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), is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Bio Tonsilla Phase is 43742-1600. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Bio Tonsilla Phase drug includes Acetylcholine Chloride - 6 [hp_X]/mL Anemone Pratensis - 6 [hp_X]/mL Antimony Potassium Tartrate - 6 [hp_X]/mL Ascorbic Acid - 6 [hp_X]/mL Barium Carbonate - 28 [hp_X]/mL Conium Maculatum Flowering Top - 8 [hp_X]/mL Cortisone Acetate - 13 [hp_X]/mL Echinacea Angustifolia - 4 [hp_X]/mL Galium Aparine - 6 [hp_X]/mL Gentiana Lutea Root - 6 [hp_X]/mL and more. The currest status of Bio Tonsilla Phase drug is Active.

Drug Information:

Drug NDC:	43742-1600
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Bio Tonsilla Phase
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
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),
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACETYLCHOLINE CHLORIDE - 6 [hp_X]/mL ANEMONE PRATENSIS - 6 [hp_X]/mL ANTIMONY POTASSIUM TARTRATE - 6 [hp_X]/mL ASCORBIC ACID - 6 [hp_X]/mL BARIUM CARBONATE - 28 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP - 8 [hp_X]/mL CORTISONE ACETATE - 13 [hp_X]/mL ECHINACEA ANGUSTIFOLIA - 4 [hp_X]/mL GALIUM APARINE - 6 [hp_X]/mL GENTIANA LUTEA ROOT - 6 [hp_X]/mL Load more... GERANIUM ROBERTIANUM - 6 [hp_X]/mL HORSE CHESTNUT - 6 [hp_X]/mL LACTIC ACID, L- - 6 [hp_X]/mL MANNOSE, D- - 6 [hp_X]/mL MERCURIUS SOLUBILIS - 13 [hp_X]/mL PORK LIVER - 10 [hp_X]/mL PROTORTONIA CACTI - 6 [hp_X]/mL SOLANUM DULCAMARA TOP - 4 [hp_X]/mL SULFUR - 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 13 [hp_X]/mL SUS SCROFA BONE MARROW - 10 [hp_X]/mL SUS SCROFA HYPOTHALAMUS - 10 [hp_X]/mL SUS SCROFA LYMPH - 8 [hp_X]/mL SUS SCROFA SPLEEN - 10 [hp_X]/mL SUS SCROFA THYROID - 13 [hp_X]/mL SUS SCROFA TONSIL - 28 [hp_X]/mL SUS SCROFA UMBILICAL CORD - 10 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE - 10 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date:	29 Oct, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	05 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000193618 M0001797
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	AF73293C2R 8E272251DI DL6OZ476V3 PQ6CK8PD0R 6P669D8HQ8 Q28R5GF371 883WKN7W8X VB06AV5US8 Z4B6561488 S72O3284MS Load more... R5I1HK0UBL 3C18L6RJAZ F9S9FFU82N PHA4727WTP 324Y4038G2 6EC706HI7F LZB7TFX1LT KPS1B1162N 70FD1KFU70 398IYQ16YV VP2CN2G7Y8 N6R0856Z79 33A7VYU29L 92AMN5J79Y 6RV024OAUQ TB08NIC03W 118OYG6W3H 91D9GV0Z28
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Vitamin C [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:	Ascorbic Acid [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Ascorbic Acid [CS] Blood Coagulation Factor [EPC] Calcium [CS] Cations Divalent [CS] Cholinergic Agonists [MoA] Cholinergic Receptor Agonist [EPC] Corticosteroid Hormone Receptor Agonists [MoA] Corticosteroid [EPC] Increased Coagulation Factor Activity [PE] Vitamin C [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1600-1	30 mL in 1 BOTTLE, DROPPER (43742-1600-1)	29 Oct, 2019	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Bio Tonsilla Phase

Dulcamara & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1600

Purpose:

Homeopathic indications: 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.

Product Elements:

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), solanum dulcamara top solanum dulcamara top echinacea angustifolia echinacea angustifolia horse chestnut horse chestnut antimony potassium tartrate antimony cation (3+) ascorbic acid ascorbic acid protortonia cacti protortonia cacti galium aparine galium aparine gentiana lutea root gentiana lutea root geranium robertianum geranium robertianum anemone pratensis anemone pratensis lactic acid, l- lactic acid, l- acetylcholine chloride acetylcholine mannose, d- mannose, d- conium maculatum flowering top conium maculatum flowering top sus scrofa lymph sus scrofa lymph sulfur sulfur tribasic calcium phosphate calcium cation sus scrofa umbilical cord sus scrofa umbilical cord pork liver pork liver sus scrofa hypothalamus sus scrofa hypothalamus sus scrofa bone marrow sus scrofa bone marrow sus scrofa spleen sus scrofa spleen cortisone acetate cortisone sus scrofa adrenal gland sus scrofa adrenal gland mercurius solubilis mercurius solubilis sus scrofa thyroid sus scrofa thyroid barium carbonate barium cation sus scrofa tonsil sus scrofa tonsil water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact a physician or poison control center right away. if pregnant or breast-feeding, ask a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing.

Dosage and Administration:

Directions: 1-10 drops under the tongue, 2 times a day or as directed by a health professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1600-1 homeopathic bio tonsilla phase 1 fl oz (30 ml) bio tonsilla phase

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.