1. Home
  2. Labeler Index
  3. Deseret Biologicals, Inc.
  4. NDC Product Code: 43742-1600 Bio Tonsilla Phase

NDC 43742-1600 Bio Tonsilla Phase

Dulcamara,Echinacea (angustifolia),Aesculus Hippocastanum,Antimonium Tartaricum,Ascorbicum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1600?
  4. Bio Tonsilla Phase Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-1600
Proprietary Name:
Bio Tonsilla Phase
Non-Proprietary Name: [1]
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: [2]
Acetylcholine Chloride; Anemone Pratensis; Antimony Potassium Tartrate; Ascorbic Acid; Barium Carbonate; Conium Maculatum Flowering Top; Cortisone Acetate; Echinacea Angustifolia; Galium Aparine; Gentiana Lutea Root; Geranium Robertianum; Horse Chestnut; Lactic Acid, L-; Mannose, D-; Mercurius Solubilis; Pork Liver; Protortonia Cacti; Solanum Dulcamara Top; Sulfur; Sus Scrofa Adrenal Gland; Sus Scrofa Bone Marrow; Sus Scrofa Hypothalamus; Sus Scrofa Lymph; Sus Scrofa Spleen; Sus Scrofa Thyroid; Sus Scrofa Tonsil; Sus Scrofa Umbilical Cord; Tribasic Calcium Phosphate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Deseret Biologicals, Inc.
    Labeler Code:
    43742
    Product Label ID:
    74f899ed-8021-470a-995b-4822da412c50
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-29-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-1600-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43742-1600?

    The NDC code 43742-1600 is assigned by the FDA to the product Bio Tonsilla Phase which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bio Tonsilla Phase is 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), . The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 43742-1600-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Bio Tonsilla Phase?

    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.

    What are Bio Tonsilla Phase Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Bio Tonsilla Phase UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Bio Tonsilla Phase Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".