Spectric

Ethylicum, Kali Bromatum, Aspartic Acid, L-dopa, Serotonin (hydrochloride), Cerebrum Suis, Placenta Totalis Suis, Agaricus Muscarius, Bufo Rana, Helleborus Niger, Hyoscyamus Niger, Olibanum (boswellia Serrata), Stramonium, Thuja Occidentalis, Helium, Neon, Carcinosin, Hydrogen

Deseret Biologicals, Inc
Human Otc Drug
NDC 43742-1177

Spectric also known as Ethylicum, Kali Bromatum, Aspartic Acid, L-dopa, Serotonin (hydrochloride), Cerebrum Suis, Placenta Totalis Suis, Agaricus Muscarius, Bufo Rana, Helleborus Niger, Hyoscyamus Niger, Olibanum (boswellia Serrata), Stramonium, Thuja Occidentalis, Helium, Neon, Carcinosin, Hydrogen is a human otc drug labeled by 'Deseret Biologicals, Inc'. National Drug Code (NDC) number for Spectric is 43742-1177. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Spectric drug includes Alcohol - 6 [hp_X]/mL Amanita Muscaria Fruiting Body - 12 [hp_X]/mL Aspartic Acid - 6 [hp_X]/mL Bufo Bufo Cutaneous Gland - 12 [hp_X]/mL Datura Stramonium - 12 [hp_X]/mL Helium - 16 [hp_X]/mL Helleborus Niger Root - 12 [hp_X]/mL Human Breast Tumor Cell - 30 [hp_X]/mL Hydrogen - 12 [hp_C]/mL Hyoscyamus Niger - 12 [hp_X]/mL and more. The currest status of Spectric drug is Active.

Drug Information:

Drug NDC:	43742-1177
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:	Spectric
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:	Ethylicum, Kali Bromatum, Aspartic Acid, L-dopa, Serotonin (hydrochloride), Cerebrum Suis, Placenta Totalis Suis, Agaricus Muscarius, Bufo Rana, Helleborus Niger, Hyoscyamus Niger, Olibanum (boswellia Serrata), Stramonium, Thuja Occidentalis, Helium, Neon, Carcinosin, Hydrogen
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:	ALCOHOL - 6 [hp_X]/mL AMANITA MUSCARIA FRUITING BODY - 12 [hp_X]/mL ASPARTIC ACID - 6 [hp_X]/mL BUFO BUFO CUTANEOUS GLAND - 12 [hp_X]/mL DATURA STRAMONIUM - 12 [hp_X]/mL HELIUM - 16 [hp_X]/mL HELLEBORUS NIGER ROOT - 12 [hp_X]/mL HUMAN BREAST TUMOR CELL - 30 [hp_X]/mL HYDROGEN - 12 [hp_C]/mL HYOSCYAMUS NIGER - 12 [hp_X]/mL Load more... INDIAN FRANKINCENSE - 12 [hp_X]/mL LEVODOPA - 6 [hp_X]/mL NEON - 16 [hp_X]/mL POTASSIUM BROMIDE - 6 [hp_X]/mL SEROTONIN HYDROCHLORIDE - 6 [hp_X]/mL SUS SCROFA CEREBRUM - 8 [hp_X]/mL SUS SCROFA PLACENTA - 8 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG - 12 [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:	20 Feb, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	01 Jul, 2027
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:	15 May, 2026
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:	N0000193220 M0370111
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	3K9958V90M DIF093I037 30KYC7MIAI Q59QU6N72Q G6W4F0V8Z3 206GF3GB41 608DGJ6815 C62OO7VD9K 7YNJ3PO35Z 4WRK2153H3 Load more... 4PW41QCO2M 46627O600J 4VB4Y46AHD OSD78555ZM GKN429M9VS 4GB5DQR532 C8CV8867O8 1NT28V9397
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:	Aromatic Amino Acid [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 CS:	Amino Acids, Aromatic [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:	Amino Acids Aromatic [CS] Aromatic Amino Acid [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
43742-1177-1	30 mL in 1 BOTTLE, DROPPER (43742-1177-1)	20 Feb, 2018	01 Jul, 2027	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

Spectric

Ethylicum & more..

Liquid
Deseret Biologicals, Inc
NDC: 43742-1177

Purpose:

Homeopathic indications: for the temporary relief of symptoms such as agitation, lack of empathy, angry outburst, repetitive behaviors, repetitive speech, delayed language development, indifferent to human interaction, and precocity.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Spectric ethylicum, kali bromatum, aspartic acid, l-dopa, serotonin (hydrochloride), cerebrum suis, placenta totalis suis, agaricus muscarius, bufo rana, helleborus niger, hyoscyamus niger, olibanum (boswellia serrata), stramonium, thuja occidentalis, helium, neon, carcinosin, hydrogen alcohol alcohol potassium bromide bromide ion aspartic acid aspartic acid levodopa levodopa serotonin hydrochloride serotonin sus scrofa cerebrum sus scrofa cerebrum sus scrofa placenta sus scrofa placenta amanita muscaria fruiting body amanita muscaria fruiting body bufo bufo cutaneous gland bufo bufo cutaneous gland helleborus niger root helleborus niger root hyoscyamus niger hyoscyamus niger indian frankincense indian frankincense datura stramonium datura stramonium thuja occidentalis leafy twig thuja occidentalis leafy twig helium helium neon neon human breast tumor cell human breast tumor cell hydrogen hydrogen water

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 43742-1177-1 homeopathic spectric 1 fl oz (30 ml) spectric

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.