NDC 43742-0628 Fng

Berberis Vulgaris, Cochlearia Armoracia, Echinacea (angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Myrrha, Tabebuia Impetiginosa, Propolis, Formalinum, Glandula Suprarenalis Suis, Thymus (suis), Ferrum Metallicum, Iridium Metallicum, Lycopodium Clavatum, Phosphoricum Acidum, Pulsatilla (vulgaris), Selenium Metallicum, Zincum Metallicum, Adenosinum Triphosphoricum Dinatrum, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Mucor Racemosus, Pullularia Pullulans

NDC Product Code 43742-0628

NDC Code: 43742-0628

Proprietary Name: Fng 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: Berberis Vulgaris, Cochlearia Armoracia, Echinacea (angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Myrrha, Tabebuia Impetiginosa, Propolis, Formalinum, Glandula Suprarenalis Suis, Thymus (suis), Ferrum Metallicum, Iridium Metallicum, Lycopodium Clavatum, Phosphoricum Acidum, Pulsatilla (vulgaris), Selenium Metallicum, Zincum Metallicum, Adenosinum Triphosphoricum Dinatrum, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Mucor Racemosus, Pullularia Pullulans 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.
    • 43742-0628 - Fng

NDC 43742-0628-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Fng with NDC 43742-0628 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Fng is berberis vulgaris, cochlearia armoracia, echinacea (angustifolia), hydrastis canadensis, lomatium dissectum, myrrha, tabebuia impetiginosa, propolis, formalinum, glandula suprarenalis suis, thymus (suis), ferrum metallicum, iridium metallicum, lycopodium clavatum, phosphoricum acidum, pulsatilla (vulgaris), selenium metallicum, zincum metallicum, adenosinum triphosphoricum dinatrum, alternaria tenuis nees, aspergillus niger, candida albicans, candida parapsilosis, mucor racemosus, pullularia pullulans. 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.

Fng 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.

  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • HORSERADISH 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • GOLDENSEAL 3 [hp_X]/mL
  • LOMATIUM DISSECTUM ROOT 3 [hp_X]/mL
  • MYRRH 3 [hp_X]/mL
  • TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
  • PROPOLIS WAX 6 [hp_X]/mL
  • FORMALDEHYDE 6 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • IRON 12 [hp_X]/mL
  • IRIDIUM 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PULSATILLA VULGARIS 12 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
  • ALTERNARIA ALTERNATA 12 [hp_X]/mL
  • ASPERGILLUS NIGER VAR. NIGER 12 [hp_X]/mL
  • CANDIDA ALBICANS 12 [hp_X]/mL
  • CANDIDA PARAPSILOSIS 12 [hp_X]/mL
  • MUCOR RACEMOSUS 12 [hp_X]/mL
  • AUREOBASIDIUM PULLULANS VAR. PULLUTANS 12 [hp_X]/mL
  • RHIZOPUS STOLONIFER 12 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE 12 [hp_X]/mL
  • METHYLCOBALAMIN 12 [hp_X]/mL
  • LACTIC ACID, L- 12 [hp_X]/mL
  • STACHYBOTRYS CHARTARUM 12 [hp_X]/mL
  • ESCHERICHIA COLI 30 [hp_C]/mL
  • BRUGIA MALAYI 39 [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: 07-21-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 10-27-2020 What is the End Marketing Date?
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.

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.

Fng Product Label Images

Fng 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:

Berberis Vulgaris 3X, Cochlearia Armoracia 3X, Echinacea (Angustifolia) 3X, Hydrastis Canadensis 3X, Lomatium Dissectum 3X, Myrrha 3X, Tabebuia Impetiginosa 3X, Propolis 6X, Formalinum 6X, 12X, 30X, 12C, 30C, 200C, Glandula Suprarenalis Suis 8X, Thymus (Suis) 8X, Ferrum Metallicum 12X, Iridium Metallicum 12X, Lycopodium Clavatum 12X, Phosphoricum Acidum 12X, Pulsatilla (Vulgaris) 12X, Selenium Metallicum 12X, Zincum Metallicum 12X, Adenosinum Triphosphoricum Dinatrum 12X, 30X, 200X, Alternaria Tenuis Nees 12X, 30X, 200X, Aspergillus Niger 12X, 30X, 200X, Candida Albicans 12X, 30X, 200X, Candida Parapsilosis 12X, 30X, 200X, Mucor Racemosus 12X, 30X, 200X, Pullularia Pullulans 12X, 30X, 200X, Rhizopus Nigricans 12X, 30X, 200X, Torula Cerevisiae 12X, 30X, 200X, Methylcobalamin 12X, 30X, 200X, Sarcolacticum Acidum 12X, 30X, 200X, Styachybotrys Chartarum 12X, 30X, 200X, Mutabile Bacillus (Bach) 30C, Brugia Malayi 39C, 60C, 200C.

Indications:

For temporary relief of symptoms related to fungal, yeast, candida and mold contamination including gastritis, constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, hyperactivity, mood swings, diarrhea, depression and dizziness.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to fungal, yeast, candida and mold contamination including gastritis, constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, hyperactivity, mood swings, diarrhea, depression and dizziness.****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 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 a physician or a Poison Control Center right away.

Directions:

1-10 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**For a complete list of Fungus Nosodes contact Deseret Biologicals, Inc.

Package Label Display:

DESBIONDC 43742-0628-1HOMEOPATHICFNG1 FL OZ (30 ml)

* Please review the disclaimer below.

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