NDC 43742-1121 Esteem

Ambra Grisea, Lilium Tigrinum, Lycopodium Clavatum, Natrum Carbonicum, Viscum Album, Thuja Occidentalis, Hypothalamus Suis, Cubeba Officinalis, Agnus Castus, Anacardium Orientale, Baryta Iodata, Lac Caninum, Lac Felinum, Naja Tripudians, Rhus Glabra, Rosa Damascena, Sabadilla, Aurum Metallicum, Magnesium Iodide, Carcinosin

NDC Product Code 43742-1121

NDC CODE: 43742-1121

Proprietary Name: Esteem 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: Ambra Grisea, Lilium Tigrinum, Lycopodium Clavatum, Natrum Carbonicum, Viscum Album, Thuja Occidentalis, Hypothalamus Suis, Cubeba Officinalis, Agnus Castus, Anacardium Orientale, Baryta Iodata, Lac Caninum, Lac Felinum, Naja Tripudians, Rhus Glabra, Rosa Damascena, Sabadilla, Aurum Metallicum, Magnesium Iodide, Carcinosin 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 43742-1121-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Esteem with NDC 43742-1121 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Esteem is ambra grisea, lilium tigrinum, lycopodium clavatum, natrum carbonicum, viscum album, thuja occidentalis, hypothalamus suis, cubeba officinalis, agnus castus, anacardium orientale, baryta iodata, lac caninum, lac felinum, naja tripudians, rhus glabra, rosa damascena, sabadilla, aurum metallicum, magnesium iodide, carcinosin. 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.

Esteem 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.

  • AMBERGRIS 6 [hp_X]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 6 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
  • SODIUM CARBONATE 6 [hp_X]/mL
  • VISCUM ALBUM FRUITING TOP 6 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • PIPER CUBEBA FRUIT 9 [hp_X]/mL
  • CHASTE TREE 12 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE 12 [hp_X]/mL
  • BARIUM IODIDE 12 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK 12 [hp_X]/mL
  • FELIS CATUS MILK 12 [hp_X]/mL
  • NAJA NAJA VENOM 12 [hp_X]/mL
  • RHUS GLABRA TOP 12 [hp_X]/mL
  • ROSA X DAMASCENA FLOWERING TOP 12 [hp_X]/mL
  • SCHOENOCAULON OFFICINALE SEED 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • MAGNESIUM IODIDE 16 [hp_X]/mL
  • HUMAN BREAST TUMOR CELL 30 [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.
  • 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: 12-19-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

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.

Esteem Product Label Images

Esteem 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:

Ambra Grisea 6X, Lilium Tigrinum 6X, Lycopodium Clavatum 6X, Natrum Carbonicum 6X, Viscum Album 6X, Thuja Occidentalis 6X, 12X, 30X, Hypothalamus (Suis) 8X, 12X, 30X, Cubeba Officinalis 9X, Agnus Castus 12X, Anacardium Orientale 12X, Baryta Iodata 12X, Lac Caninum 12X, Lac Felinum 12X, Naja Tripudians 12X, Rhus Glabra 12X, Rosa Damascena 12X, Sabadilla 12X, Aurum Metallicum 12X, 30X, Magnesium Iodide 16X, Carcinosinum 30X.

Homeopathic Indications:

For the temporary relief of the symptoms related to lack of self-esteem including codependency lack of self-confidence and narcissism.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of the symptoms related to lack of self-esteem including codependency lack of self-confidence and narcissism.****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 43742-1121-1HOMEOPATHICENTSUPPORT1 FL OZ (30 ml)

* Please review the disclaimer below.