NDC 43742-1115 Focus

Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Formicum Acidum, Malicum Acidum, Sarcolacticum Acid, Dulcamara, Hyoscyamus Niger, Phosphorus, Sabina, Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba(gamma-aminobutyric Acid), Norepinephrine, Octopamine (hydrochloride), Phenylethylamine (hydrochloride), Serotonin (hydrochloride), Taurine, Tyramine, Adenosinum Cyclophosphoricum, Brain Stem (suis), Cerebrum Suis, Diencephalon (suis), Pineal Gland (suis)

NDC Product Code 43742-1115

NDC Code: 43742-1115

Proprietary Name: Focus 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: Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Formicum Acidum, Malicum Acidum, Sarcolacticum Acid, Dulcamara, Hyoscyamus Niger, Phosphorus, Sabina, Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba(gamma-aminobutyric Acid), Norepinephrine, Octopamine (hydrochloride), Phenylethylamine (hydrochloride), Serotonin (hydrochloride), Taurine, Tyramine, Adenosinum Cyclophosphoricum, Brain Stem (suis), Cerebrum Suis, Diencephalon (suis), Pineal Gland (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.
    • 43742-1115 - Focus

NDC 43742-1115-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Focus with NDC 43742-1115 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Focus is adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, formicum acidum, malicum acidum, sarcolacticum acid, dulcamara, hyoscyamus niger, phosphorus, sabina, acetylcholine chloride, adrenalinum, dopamine hydrochloride, gaba(gamma-aminobutyric acid), norepinephrine, octopamine (hydrochloride), phenylethylamine (hydrochloride), serotonin (hydrochloride), taurine, tyramine, adenosinum cyclophosphoricum, brain stem (suis), cerebrum suis, diencephalon (suis), pineal gland (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.

Focus 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.

  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
  • OXOGLURIC ACID 6 [hp_X]/mL
  • FORMIC ACID 6 [hp_X]/mL
  • MALIC ACID 6 [hp_X]/mL
  • LACTIC ACID, L- 6 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 6 [hp_X]/mL
  • HYOSCYAMUS NIGER 6 [hp_X]/mL
  • PHOSPHORUS 6 [hp_X]/mL
  • JUNIPERUS SABINA LEAFY TWIG 6 [hp_X]/mL
  • ACETYLCHOLINE CHLORIDE 6 [hp_X]/mL
  • EPINEPHRINE 6 [hp_X]/mL
  • DOPAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]/mL
  • NOREPINEPHRINE 6 [hp_X]/mL
  • OCTOPAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • PHENETHYLAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 6 [hp_X]/mL
  • TAURINE 6 [hp_X]/mL
  • TYRAMINE 6 [hp_X]/mL
  • ADENOSINE CYCLIC PHOSPHATE 8 [hp_X]/mL
  • SUS SCROFA BRAINSTEM 8 [hp_X]/mL
  • SUS SCROFA CEREBRUM 8 [hp_X]/mL
  • SUS SCROFA DIENCEPHALON 8 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 8 [hp_X]/mL
  • SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 30 [hp_C]/mL
  • STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/mL
  • LYCOSA TARANTULA 30 [hp_C]/mL
  • VALERIAN 30 [hp_C]/mL
  • VERATRUM ALBUM ROOT 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: 12-12-2017 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: 01-18-2023 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.

Focus Product Label Images

Focus 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:

Adenosinum Triphosphoricum Dinatrum 6X, Alpha-Ketoglutaricum Acidum 6X, Formicum Acidum 6X, Malicum Acidum 6X, Sarcolacticum Acid 6X, Dulcamara 6X, 12X, 30X, Hyoscyamus Niger 6X, 12X, 30X, Phosphorus 6X, 12X, 30X, Sabina 6X, 12X, 30X, Acetylcholine Chloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adrenalinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Dopamine Hydrochloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, GABA(Gamma-Aminobutyric Acid) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Norepinephrine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Octopamine (Hydrochloride) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Phenylethylamine (Hydrochloride) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Serotonin (Hydrochloride) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Taurine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Tyramine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Cyclophosphoricum 8X, Brain Stem (Suis) 8X, Cerebrum Suis 8X, Diencephalon (Suis) 8X, Pineal Gland (Suis) 8X, Thalamus Opticus (Suis) 8X, Silicea 8X, 12X, 30X, Arsenicum Album 30C, Dysentery Bacillus 30C, Nux Vomica 30C, Tarentula Hispana 30C, Valeriana Officinalis 30C, Veratrum Album 30C.

Homeopathic Indications:

For temporary relief of symptoms related to poor concentration.****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 poor concentration.****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:

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 43742-0733-1HOMEOPATHICFOCUS1 FL OZ (30 ml)

* Please review the disclaimer below.

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