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

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1121

Esteem also known as 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 is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Esteem is 43742-1121. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Esteem drug includes Ambergris - 6 [hp_X]/mL Barium Iodide - 12 [hp_X]/mL Canis Lupus Familiaris Milk - 12 [hp_X]/mL Chaste Tree - 12 [hp_X]/mL Felis Catus Milk - 12 [hp_X]/mL Gold - 12 [hp_X]/mL Human Breast Tumor Cell - 30 [hp_X]/mL Lilium Lancifolium Whole Flowering - 6 [hp_X]/mL Lycopodium Clavatum Spore - 6 [hp_X]/mL Magnesium Iodide - 16 [hp_X]/mL and more. The currest status of Esteem drug is Active.

Drug Information:

Drug NDC:	43742-1121
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Esteem
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
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
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	AMBERGRIS - 6 [hp_X]/mL BARIUM IODIDE - 12 [hp_X]/mL CANIS LUPUS FAMILIARIS MILK - 12 [hp_X]/mL CHASTE TREE - 12 [hp_X]/mL FELIS CATUS MILK - 12 [hp_X]/mL GOLD - 12 [hp_X]/mL HUMAN BREAST TUMOR CELL - 30 [hp_X]/mL LILIUM LANCIFOLIUM WHOLE FLOWERING - 6 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 6 [hp_X]/mL MAGNESIUM IODIDE - 16 [hp_X]/mL Load more... NAJA NAJA VENOM - 12 [hp_X]/mL PIPER CUBEBA FRUIT - 9 [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 SEMECARPUS ANACARDIUM JUICE - 12 [hp_X]/mL SODIUM CARBONATE - 6 [hp_X]/mL SUS SCROFA HYPOTHALAMUS - 8 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG - 6 [hp_X]/mL VISCUM ALBUM FRUITING TOP - 6 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	19 Dec, 2017
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	12 Jun, 2026
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185508 N0000175629 N0000184306 M0000728
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	XTC0D02P6C WKC4T7680A G39P120JQT 433OSF3U8A 5A3Y60049Z 79Y1949PYO C62OO7VD9K X67Z2963PI C88X29Y479 W74QE3H320 Load more... ZZ4AG7L7VM Z99L7429MA RHH784E0K6 21W82Q764G 6NAF1689IO Y0F0BU8RDU 45P3261C7T N6R0856Z79 1NT28V9397 BK9092J5MP
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Chemical Allergen [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Standardized Chemical Allergen [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1121-1	30 mL in 1 BOTTLE, DROPPER (43742-1121-1)	19 Dec, 2017	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Esteem

Ambra Grisea & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1121

Purpose:

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.

Product Elements:

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 ambergris ambergris lilium lancifolium whole flowering lilium lancifolium whole flowering lycopodium clavatum spore lycopodium clavatum spore sodium carbonate carbonate ion viscum album fruiting top viscum album fruiting top thuja occidentalis leafy twig thuja occidentalis leafy twig sus scrofa hypothalamus sus scrofa hypothalamus piper cubeba fruit piper cubeba fruit chaste tree chaste tree semecarpus anacardium juice semecarpus anacardium juice barium iodide barium cation canis lupus familiaris milk canis lupus familiaris milk felis catus milk felis catus milk naja naja venom naja naja venom rhus glabra top rhus glabra top rosa x damascena flowering top rosa x damascena flowering top schoenocaulon officinale seed schoenocaulon officinale seed gold gold magnesium iodide magnesium iodide human breast tumor cell human breast tumor cell water alcohol

Indications and Usage:

Warnings:

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.

Dosage and Administration:

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.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1121-1 homeopathic esteem 1 fl oz (30 ml) esteem

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.