NDC 43742-1600 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),

NDC Product Code 43742-1600

NDC Code: 43742-1600

Proprietary Name: Bio Tonsilla Phase What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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), 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.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1600-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bio Tonsilla Phase with NDC 43742-1600 is a 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.

Labeler Name: Deseret Biologicals, Inc.

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.

Product Type: Human Otc Drug 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.

Bio Tonsilla Phase Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SOLANUM DULCAMARA TOP 4 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 4 [hp_X]/mL
  • HORSE CHESTNUT 6 [hp_X]/mL
  • ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • PROTORTONIA CACTI 6 [hp_X]/mL
  • GALIUM APARINE 6 [hp_X]/mL
  • GENTIANA LUTEA ROOT 6 [hp_X]/mL
  • GERANIUM ROBERTIANUM 6 [hp_X]/mL
  • ANEMONE PRATENSIS 6 [hp_X]/mL
  • LACTIC ACID, L- 6 [hp_X]/mL
  • ACETYLCHOLINE CHLORIDE 6 [hp_X]/mL
  • MANNOSE, D- 6 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 8 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 10 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 10 [hp_X]/mL
  • PORK LIVER 10 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 10 [hp_X]/mL
  • SUS SCROFA BONE MARROW 10 [hp_X]/mL
  • SUS SCROFA SPLEEN 10 [hp_X]/mL
  • CORTISONE ACETATE 13 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 13 [hp_X]/mL
  • MERCURIUS SOLUBILIS 13 [hp_X]/mL
  • SUS SCROFA THYROID 13 [hp_X]/mL
  • BARIUM CARBONATE 28 [hp_X]/mL
  • SUS SCROFA TONSIL 28 [hp_X]/mL

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 10-29-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Bio Tonsilla Phase Product Label Images