43742-1177 NDC - 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)

Drug Information

  • Product NDC: 43742-1177
  • Proprietary Name: Spectric
  • 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
  • Active Ingredient(s): 6 [hp_X]/mL ALCOHOL; 12 [hp_X]/mL AMANITA MUSCARIA FRUITING BODY; 6 [hp_X]/mL ASPARTIC ACID; 12 [hp_X]/mL BUFO BUFO CUTANEOUS GLAND; 12 [hp_X]/mL DATURA STRAMONIUM; 16 [hp_X]/mL HELIUM; 12 [hp_X]/mL HELLEBORUS NIGER ROOT; 30 [hp_X]/mL HUMAN BREAST TUMOR CELL; 12 [hp_C]/mL HYDROGEN; 12 [hp_X]/mL HYOSCYAMUS NIGER; 12 [hp_X]/mL INDIAN FRANKINCENSE; 6 [hp_X]/mL LEVODOPA; 16 [hp_X]/mL NEON; 6 [hp_X]/mL POTASSIUM BROMIDE; 6 [hp_X]/mL SEROTONIN HYDROCHLORIDE; 8 [hp_X]/mL SUS SCROFA CEREBRUM; 8 [hp_X]/mL SUS SCROFA PLACENTA; 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Amino Acids; Aromatic [CS]; Aromatic Amino Acid [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/20/2018
End Marketing Date:7/1/2027

Package Information

No. Package Code Package Description Billing Unit
143742-1177-130 mL in 1 BOTTLE, DROPPER (43742-1177-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1177The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMESpectricThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEthylicum, 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, HydrogenThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/20/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE7/1/2027This 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.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEDeseret Biologicals, IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALCOHOL; AMANITA MUSCARIA FRUITING BODY; ASPARTIC ACID; BUFO BUFO CUTANEOUS GLAND; DATURA STRAMONIUM; HELIUM; HELLEBORUS NIGER ROOT; HUMAN BREAST TUMOR CELL; HYDROGEN; HYOSCYAMUS NIGER; INDIAN FRANKINCENSE; LEVODOPA; NEON; POTASSIUM BROMIDE; SEROTONIN HYDROCHLORIDE; SUS SCROFA CEREBRUM; SUS SCROFA PLACENTA; THUJA OCCIDENTALIS LEAFY TWIGAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6; 12; 6; 12; 12; 16; 12; 30; 12; 12; 12; 6; 16; 6; 6; 8; 8; 12 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC] 

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This page was last updated on: 11/21/2025

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