NDC 43742-1575 Fng

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

NDC Product Code 43742-1575

NDC CODE: 43742-1575

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), Lomatium Dissectum, Myrrha, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Tabebuia Impetiginosa, Thymus (suis), Formalinum, Carbolicum Acidum, Ferrum Metallicum, Iridium Metallicum, Lycopodium Clavatum, Phosphoricum Acidum, Pulsatilla (prastensis), Selenium Metallicum, Zincum Metallicum, Adenosinum Triphosphoricum Dinatrum, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Torula Cerevisiae, 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used as an antiperspirant to treat feet that sweat or smell excessively. It is also used as a drying agent during wart treatment.
  • This medication is an iron supplement used to treat or prevent low blood levels of iron (e.g., for anemia or during pregnancy). Iron is an important mineral that the body needs to produce red blood cells and keep you in good health.
  • Drug uses not available
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1575-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Fng with NDC 43742-1575 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), lomatium dissectum, myrrha, hydrastis canadensis, propolis, glandula suprarenalis suis, tabebuia impetiginosa, thymus (suis), formalinum, carbolicum acidum, ferrum metallicum, iridium metallicum, lycopodium clavatum, phosphoricum acidum, pulsatilla (prastensis), selenium metallicum, zincum metallicum, adenosinum triphosphoricum dinatrum, alternaria tenuis nees, aspergillus niger, candida albicans, candida parapsilosis, torula cerevisiae, . 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
  • LOMATIUM DISSECTUM ROOT 3 [hp_X]/mL
  • MYRRH 3 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • PROPOLIS WAX 6 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • TABEBUIA IMPETIGINOSA BARK 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • FORMALDEHYDE 8 [hp_X]/mL
  • PHENOL 12 [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
  • ANEMONE PRATENSIS 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
  • SACCHAROMYCES CEREVISIAE 12 [hp_X]/mL
  • METHYLCOBALAMIN 12 [hp_X]/mL
  • LACTIC ACID, L- 12 [hp_X]/mL
  • MUCOR RACEMOSUS 16 [hp_C]/mL
  • RHIZOPUS STOLONIFER 14 [hp_C]/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.
  • 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: 10-01-2019 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.

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, Lomatium Dissectum 3X, Myrrha 3X, Hydrastis Canadensis 6X, Propolis 6X, Glandula Suprarenalis Suis 8X, Tabebuia Impetiginosa 8X, Thymus (Suis) 8X, Formalinum 8X, 12X, 30X, 12C, 30C, 200C, Carbolicum acidum 12X, Ferrum Metallicum 12X, Iridium Metallicum 12X, Lycopodium Clavatum 12X, Phosphoricum Acidum 12X, Pulsatilla (Prastensis) 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, Torula Cerevisiae 12X, 30X, 200X, Methylcobalamin 12X, 30X, 200X, Sarcolacticum Acidum 12X, 30X, 200X, Mucor Racemosus 16X, 30X, 300X, Rhizopus Nigricans 14C, 30C, 200C, Mutabile Bacillus (Bach) 30C, Brugia Malayi 39C, 60C, 200C.

Homeopathic Indications:

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

For temporary relief of symptoms related to yeast, including occasional constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, mood swings, occasional diarrhea and dizziness.****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 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 a physician or 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

Package Label Display:

DESBIONDC 43742-1285-1HOMEOPATHICFNG1 FL OZ (30 ml)

* Please review the disclaimer below.