NDC 43742-1394 Energize

Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosus, Galium Aparine, Thyroidinum (suis), Dhea (dehydroepiandrosterone), Phenyl Isothiocyanate, Tyramine, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Fumaricum Acidum, Malic Acidum, Colchicum Autumnale, Conium Maculatum, Natrum Oxalaceticum, Funiculus Umbilicalis Suis, Hepar Suis, Medulla Ossis Suis, Pineal Gland (suis), Spleen (suis), Thymus (suis), Calcarea Fluorica, Pulsatilla (vulgaris), Spongia Tosta, Cortisone Aceticum

NDC Product Code 43742-1394

NDC Code: 43742-1394

Proprietary Name: Energize 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: Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosus, Galium Aparine, Thyroidinum (suis), Dhea (dehydroepiandrosterone), Phenyl Isothiocyanate, Tyramine, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Fumaricum Acidum, Malic Acidum, Colchicum Autumnale, Conium Maculatum, Natrum Oxalaceticum, Funiculus Umbilicalis Suis, Hepar Suis, Medulla Ossis Suis, Pineal Gland (suis), Spleen (suis), Thymus (suis), Calcarea Fluorica, Pulsatilla (vulgaris), Spongia Tosta, Cortisone Aceticum 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
    • 43742-1394 - Energize

NDC 43742-1394-1

Package Description: 90 TABLET in 1 BOTTLE

NDC Product Information

Energize with NDC 43742-1394 is a a human over the counter drug product labeled by Deseret Biologicals. The generic name of Energize is sarcolacticum acidum, viscum album, iodium, fucus vesiculosus, galium aparine, thyroidinum (suis), dhea (dehydroepiandrosterone), phenyl isothiocyanate, tyramine, adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, fumaricum acidum, malic acidum, colchicum autumnale, conium maculatum, natrum oxalaceticum, funiculus umbilicalis suis, hepar suis, medulla ossis suis, pineal gland (suis), spleen (suis), thymus (suis), calcarea fluorica, pulsatilla (vulgaris), spongia tosta, cortisone aceticum. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Deseret Biologicals

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Energize 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.

  • LACTIC ACID, L- 3 [hp_X]/1
  • VISCUM ALBUM FRUITING TOP 3 [hp_X]/1
  • IODINE 3 [hp_X]/1
  • FUCUS VESICULOSUS 6 [hp_X]/1
  • GALIUM APARINE 6 [hp_X]/1
  • SUS SCROFA THYROID 6 [hp_X]/1
  • PRASTERONE 6 [hp_X]/1
  • PHENYL ISOTHIOCYANATE 6 [hp_X]/1
  • TYRAMINE 6 [hp_X]/1
  • ADENOSINE TRIPHOSPHATE DISODIUM 7 [hp_X]/1
  • OXOGLURIC ACID 7 [hp_X]/1
  • FUMARIC ACID 7 [hp_X]/1
  • MALIC ACID 7 [hp_X]/1
  • COLCHICUM AUTUMNALE BULB 8 [hp_X]/1
  • CONIUM MACULATUM FLOWERING TOP 8 [hp_X]/1
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/1
  • SUS SCROFA UMBILICAL CORD 8 [hp_X]/1
  • PORK LIVER 8 [hp_X]/1
  • SUS SCROFA BONE MARROW 8 [hp_X]/1
  • SUS SCROFA PINEAL GLAND 8 [hp_X]/1
  • SUS SCROFA SPLEEN 8 [hp_X]/1
  • SUS SCROFA THYMUS 8 [hp_X]/1
  • CALCIUM FLUORIDE 12 [hp_X]/1
  • ANEMONE PULSATILLA 12 [hp_X]/1
  • SPONGIA OFFICINALIS SKELETON, ROASTED 12 [hp_X]/1
  • CORTISONE ACETATE 30 [hp_X]/1
  • MERCURIC CHLORIDE 60 [hp_X]/1
  • LIOTHYRONINE 15 [hp_C]/1
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/1
  • ESCHERICHIA COLI 30 [hp_C]/1

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.

  • LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

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
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: 09-26-2018 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: 12-31-2019 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.

Energize Product Label Images

Energize 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:

Sarcolacticum Acidum 3X, Viscum Album 3X, Iodium 3X, 6X, 12X, 30X, Fucus Vesiculosus 6X, Galium Aparine 6X, Thyroidinum (Suis) 6X, 12X, 30X, DHEA (Dehydroepiandrosterone) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Phenyl Isothiocyanate 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Tyramine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Triphosphoricum Dinatrum 7X, Alpha-Ketoglutaricum Acidum 7X, Fumaricum Acidum 7X, Malic Acidum 7X, Colchicum Autumnale 8X, Conium Maculatum 8X, Natrum Oxalaceticum 8X, Funiculus Umbilicalis Suis 8X, 12X, 30X, Hepar Suis 8X, 12X, 30X, Medulla Ossis Suis 8X, 12X, 30X, Pineal Gland (Suis) 8X, 12X, 30X, Spleen (Suis) 8X, 12X, 30X, Thymus (Suis) 8X, 12X, 30X, Calcarea Fluorica 12X, Pulsatilla (Vulgaris) 12X, Spongia Tosta 12X, Cortisone Aceticum 30X, Mercurius Corrosivus 60X, 100X, 200X, Tri-Iodothyronine 6X, 12X, 30X, 200X, 15C, 30C, 60C, 200C, Gaertner Bacillus (Bach) 30C, Mutabile Bacillus (Bach) 30C.

Homeopathic Indications:

For temporary relief of symptoms related to the thyroid system.****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 the thyroid system.****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 a physician or Poison Control Center right away.

Directions:

One tablet three times daily or as directed by a health professional.

Inactive Ingredients:

Lactose, Magnesium Stearate, Microcrystalline Cellulose.

Questions:

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

Package Label Display:

DESBIONDC 43742-1394-1HOMEOPATHICENERGIZE90 TABLETS

* Please review the disclaimer below.

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