NDC 43742-1487 Matrix Support

Ceanothus Americanus, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Pulsatilla (pratensis), Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectal Mucosa (suis), Stomach (suis), Sulphur, Veratrum Album, Mannose, Anacardium Orientale, Kreosotum,

NDC Product Code 43742-1487

NDC Code: 43742-1487

Proprietary Name: Matrix Support 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: Ceanothus Americanus, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Pulsatilla (pratensis), Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectal Mucosa (suis), Stomach (suis), Sulphur, Veratrum Album, Mannose, Anacardium Orientale, Kreosotum, 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.
    • 43742-1487 - Matrix Support

NDC 43742-1487-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Matrix Support with NDC 43742-1487 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Matrix Support is ceanothus americanus, argentum nitricum, condurango, hydrastis canadensis, momordica balsamina, pulsatilla (pratensis), bile duct (suis), colon (suis), duodenum (suis), esophagus (suis), eye (suis), gallbladder (suis), ileum (suis), intestine (suis), ipecacuanha, jejunum (suis), kali bichromicum, lung (suis), mucosa nasalis suis, natrum oxalaceticum, oral mucosa (suis), pancreas suis, phosphorus, rectal mucosa (suis), stomach (suis), sulphur, veratrum album, mannose, anacardium orientale, kreosotum,. 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.

Matrix Support 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.

  • CEANOTHUS AMERICANUS LEAF 4 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • MARSDENIA CONDURANGO BARK 6 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • MOMORDICA BALSAMINA IMMATURE FRUIT 6 [hp_X]/mL
  • ANEMONE PRATENSIS 6 [hp_X]/mL
  • SUS SCROFA BILE DUCT 8 [hp_X]/mL
  • SUS SCROFA COLON 8 [hp_X]/mL
  • SUS SCROFA DUODENUM 8 [hp_X]/mL
  • SUS SCROFA ESOPHAGUS 8 [hp_X]/mL
  • SUS SCROFA EYE 8 [hp_X]/mL
  • SUS SCROFA GALLBLADDER 8 [hp_X]/mL
  • SUS SCROFA ILEUM 8 [hp_X]/mL
  • PORK INTESTINE 8 [hp_X]/mL
  • IPECAC 8 [hp_X]/mL
  • SUS SCROFA JEJUNUM 8 [hp_X]/mL
  • POTASSIUM DICHROMATE 8 [hp_X]/mL
  • SUS SCROFA LUNG 8 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA 8 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/mL
  • SUS SCROFA ORAL MUCOSA 8 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • PHOSPHORUS 8 [hp_X]/mL
  • SUS SCROFA RECTAL MUCOSA 8 [hp_X]/mL
  • SUS SCROFA STOMACH 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • VERATRUM ALBUM ROOT 8 [hp_X]/mL
  • MANNOSE, D- 8 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE 9 [hp_X]/mL
  • WOOD CREOSOTE 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • MANDRAGORA OFFICINARUM ROOT 10 [hp_X]/mL
  • OXALIS ACETOSELLA LEAF 10 [hp_X]/mL
  • SUS SCROFA URINARY BLADDER 6 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

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: 05-16-2019 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.

Matrix Support Product Label Images

Matrix Support Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Ceanothus Americanus 4X, Argentum Nitricum 6X, Condurango 6X, Hydrastis Canadensis 6X, Momordica Balsamina 6X, Pulsatilla (Pratensis) 6X, Bile Duct (Suis) 8X, Colon (Suis) 8X, Duodenum (Suis) 8X, Esophagus (Suis) 8X, Eye (Suis) 8X, Gallbladder (Suis) 8X, Ileum (Suis) 8X, Intestine (Suis) 8X, Ipecacuanha 8X, Jejunum (Suis) 8X, Kali Bichromicum 8X, Lung, (Suis) 8X, Mucosa Nasalis Suis 8X, Natrum Oxalaceticum 8X, Oral Mucosa (Suis) 8X, Pancreas Suis 8X, Phosphorus 8X, Rectal Mucosa (Suis) 8X, Stomach (Suis) 8X, Sulphur 8X, Veratrum Album 8X, Mannose 8X, 30X, 200X, Anacardium Orientale 9X, Kreosotum 10X, Lachesis Mutus 10X, Mandragora Officinarum 10X, Oxalis Acetosella 10X, Urinary Bladder (Suis) 6C, Dysentery Bacillus 30C, 200C.

Homeopathic Indications:

For the temporary relief of symptoms such as occasional diarrhea, occasional constipation, headaches, gas, congestion, irritated eyes, and indigestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms such as occasional diarrhea, occasional constipation, headaches, gas, congestion, irritated eyes, and indigestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a 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.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1487-1HOMEOPATHICMATRIXSUPPORT1 FL OZ (30 ml)

* Please review the disclaimer below.

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