NDC 43742-1257 Bio Glyoxal Phase

Arnica Montana, Baptisia Tinctoria, Echinacea (angustifolia), Sanguinaria Canadensis, Eupatorium Perfoliatum, Euphorbium Officinarum, Dopamine Hydrochloride, Phytolacca Decandra, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Pulsatilla (pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Cortisone Aceticum, Acetaldehyde, Formalinum, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum

NDC Product Code 43742-1257

NDC Code: 43742-1257

Proprietary Name: Bio Glyoxal 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: Arnica Montana, Baptisia Tinctoria, Echinacea (angustifolia), Sanguinaria Canadensis, Eupatorium Perfoliatum, Euphorbium Officinarum, Dopamine Hydrochloride, Phytolacca Decandra, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Pulsatilla (pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Cortisone Aceticum, Acetaldehyde, Formalinum, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum 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 43742-1257-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bio Glyoxal Phase with NDC 43742-1257 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bio Glyoxal Phase is arnica montana, baptisia tinctoria, echinacea (angustifolia), sanguinaria canadensis, eupatorium perfoliatum, euphorbium officinarum, dopamine hydrochloride, phytolacca decandra, aconitum napellus, argentum nitricum, arsenicum album, bryonia (alba), gelsemium sempervirens, mercurius corrosivus, phosphorus, pulsatilla (pratensis), rhus tox, sulphur, thuja occidentalis, cortisone aceticum, acetaldehyde, formalinum, hepar sulphuris calcareum, lachesis mutus, zincum metallicum. 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 Glyoxal 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.

  • ARNICA MONTANA 4 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 4 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 5 [hp_X]/mL
  • SANGUINARIA CANADENSIS ROOT 5 [hp_X]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/mL
  • EUPHORBIA RESINIFERA RESIN 6 [hp_X]/mL
  • DOPAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 7 [hp_X]/mL
  • ACONITUM NAPELLUS 8 [hp_X]/mL
  • SILVER NITRATE 8 [hp_X]/mL
  • ARSENIC TRIOXIDE 8 [hp_X]/mL
  • BRYONIA ALBA ROOT 8 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 8 [hp_X]/mL
  • MERCURIC CHLORIDE 8 [hp_X]/mL
  • PHOSPHORUS 8 [hp_X]/mL
  • ANEMONE PRATENSIS 8 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 8 [hp_X]/mL
  • CORTISONE ACETATE 8 [hp_X]/mL
  • ACETALDEHYDE 10 [hp_X]/mL
  • FORMALDEHYDE 10 [hp_X]/mL
  • CALCIUM SULFIDE 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • ZINC 10 [hp_X]/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: 06-07-2019 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 Glyoxal Phase Product Label Images

Bio Glyoxal Phase 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:

Arnica Montana 4X, Baptisia Tinctoria 4X, Echinacea (Angustifolia) 5X, Sanguinaria Canadensis 5X, Eupatorium Perfoliatum 6X, Euphorbium Officinarum 6X, Dopamine Hydrochloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Phytolacca Decandra 7X, Aconitum Napellus 8X, Argentum Nitricum 8X, Arsenicum Album 8X, Bryonia (Alba) 8X, Gelsemium Sempervirens 8X, Mercurius Corrosivus 8X, Phosphorus 8X, Pulsatilla (Pratensis) 8X, Rhus Tox 8X, Sulphur 8X, Thuja Occidentalis 8X, Cortisone Aceticum 8X, 12X, 13X, 30X, 200X, 12C, 30C, 60C, 200C, Acetaldehyde 10X, Formalinum 10X, Hepar Sulphuris Calcareum 10X, Lachesis Mutus 10X, Zincum Metallicum 10X.

Homeopathic Indications:

For the temporary relief of symptoms of viral diseases such as colds and flu, including low energy.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms of viral diseases such as colds and flu, including low energy.****These statements are based upon 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 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.

Keep Out Of Reach Of Children:

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

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.

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 43742-1257-1HOMEOPATHICBIO GLYOXALPHASE1 FL OZ (30 ml)

* Please review the disclaimer below.