43742-1589 NDC - DAIRY ALLERGEN MIX (ADENOSINUM TRIPHOSPHORICUM DINATRUM, BENZOICUM ACIDUM, CHOLINUM, CINNAMIC ACID, EUGENOL, FOLIC ACID, FORMALINUM, HISTAMINUM HYDROCHLORICUM, L-ASPARAGINE (MONOHYDRATE), LAC DEFLORATUM, LAC VACCINUM, MENADIONE, OOPHORINUM (SUIS), PETROSELINUM SATIVUM, PHENYL ISOTHIOCYANATE, QUERCETIN, RUTIN, SACCHARUM LACTIS, ILEUM (SUIS), JEJUNUM (SUIS), STOMACH (SUIS), COUMARINUM, FOLLICULINUM, GABA (GAMMA-AMINOBUTYRIC ACID), SARCOLACTICUM ACIDUM, LAC CANINUM, LAC FELINUM, LAC HUMANUM, PIPERINE, CALCAREA CARBONICA,)

Drug Information

  • Product NDC: 43742-1589
  • Proprietary Name: Dairy Allergen Mix
  • Non Proprietary Name: Adenosinum Triphosphoricum Dinatrum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Eugenol, Folic Acid, Formalinum, Histaminum Hydrochloricum, L-Asparagine (Monohydrate), Lac Defloratum, Lac Vaccinum, Menadione, Oophorinum (Suis), Petroselinum Sativum, Phenyl Isothiocyanate, Quercetin, Rutin, Saccharum Lactis, Ileum (Suis), Jejunum (Suis), Stomach (Suis), Coumarinum, Folliculinum, GABA (Gamma-Aminobutyric Acid), Sarcolacticum Acidum, Lac Caninum, Lac Felinum, Lac Humanum, Piperine, Calcarea Carbonica,
  • Active Ingredient(s): 8 [hp_X]/mL .GAMMA.-AMINOBUTYRIC ACID; 6 [hp_C]/mL ACTIVATED CHARCOAL; 4 [hp_X]/mL ADENOSINE TRIPHOSPHATE DISODIUM; 6 [hp_X]/mL ASPARAGINE MONOHYDRATE; 6 [hp_X]/mL BENZOIC ACID; 6 [hp_C]/mL CALCIUM CITRATE; 6 [hp_C]/mL CALCIUM FLUORIDE; 6 [hp_C]/mL CALCIUM GLUCONATE; 30 [hp_X]/mL CANIS LUPUS FAMILIARIS MILK; 6 [hp_X]/mL CHOLINE HYDROXIDE; 6 [hp_X]/mL CINNAMIC ACID; 8 [hp_X]/mL COUMARIN; 6 [hp_X]/mL COW MILK; 8 [hp_X]/mL ESTRONE; 6 [hp_X]/mL EUGENOL; 30 [hp_X]/mL FELIS CATUS MILK; 6 [hp_X]/mL FOLIC ACID; 6 [hp_X]/mL FORMALDEHYDE; 6 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE; 30 [hp_X]/mL HUMAN MILK; 8 [hp_X]/mL LACTIC ACID, L-; 6 [hp_X]/mL LACTOSE, UNSPECIFIED FORM; 6 [hp_C]/mL MATRICARIA RECUTITA; 6 [hp_X]/mL MENADIONE; 6 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 6 [hp_X]/mL PETROSELINUM CRISPUM; 6 [hp_X]/mL PHENYL ISOTHIOCYANATE; 30 [hp_X]/mL PIPERINE; 6 [hp_X]/mL QUERCETIN; 6 [hp_X]/mL RUTIN; 6 [hp_C]/mL SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; 6 [hp_X]/mL SKIM MILK; 8 [hp_X]/mL SUS SCROFA ILEUM; 8 [hp_X]/mL SUS SCROFA JEJUNUM; 6 [hp_X]/mL SUS SCROFA OVARY; 8 [hp_X]/mL SUS SCROFA STOMACH; 6 [hp_C]/mL TOXICODENDRON PUBESCENS LEAF; 6 [hp_C]/mL TRIBASIC CALCIUM PHOSPHATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Ammonium Ion Binding Activity [MoA]; Blood Coagulation Factor [EPC]; Blood Coagulation Factor [EPC]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calcium [CS]; Calcium [CS]; Cations; Divalent [CS]; Cations; Divalent [CS]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Coagulation Factor Activity [PE]; Increased Coagulation Factor Activity [PE]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Milk Proteins [CS]; Nitrogen Binding Agent [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Phosphate Binder [EPC]; Phosphate Binder [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Phosphate Chelating Activity [MoA]; Phosphate Chelating Activity [MoA]; Standardized Chemical Allergen [EPC]; Standardized Chemical Allergen [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:10/25/2019
End Marketing Date:1/4/2029

Package Information

No. Package Code Package Description Billing Unit
143742-1589-130 mL in 1 BOTTLE, DROPPER (43742-1589-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1589The 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 NAMEDairy Allergen MixThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdenosinum Triphosphoricum Dinatrum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Eugenol, Folic Acid, Formalinum, Histaminum Hydrochloricum, L-Asparagine (Monohydrate), Lac Defloratum, Lac Vaccinum, Menadione, Oophorinum (Suis), Petroselinum Sativum, Phenyl Isothiocyanate, Quercetin, Rutin, Saccharum Lactis, Ileum (Suis), Jejunum (Suis), Stomach (Suis), Coumarinum, Folliculinum, GABA (Gamma-Aminobutyric Acid), Sarcolacticum Acidum, Lac Caninum, Lac Felinum, Lac Humanum, Piperine, Calcarea Carbonica,The 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 DATE10/25/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/4/2029This 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, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.GAMMA.-AMINOBUTYRIC ACID; ACTIVATED CHARCOAL; ADENOSINE TRIPHOSPHATE DISODIUM; ASPARAGINE MONOHYDRATE; BENZOIC ACID; CALCIUM CITRATE; CALCIUM FLUORIDE; CALCIUM GLUCONATE; CANIS LUPUS FAMILIARIS MILK; CHOLINE HYDROXIDE; CINNAMIC ACID; COUMARIN; COW MILK; ESTRONE; EUGENOL; FELIS CATUS MILK; FOLIC ACID; FORMALDEHYDE; HISTAMINE DIHYDROCHLORIDE; HUMAN MILK; LACTIC ACID, L-; LACTOSE, UNSPECIFIED FORM; MATRICARIA RECUTITA; MENADIONE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PETROSELINUM CRISPUM; PHENYL ISOTHIOCYANATE; PIPERINE; QUERCETIN; RUTIN; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SKIM MILK; SUS SCROFA ILEUM; SUS SCROFA JEJUNUM; SUS SCROFA OVARY; SUS SCROFA STOMACH; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATEAn 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 STRENGTH8; 6; 4; 6; 6; 6; 6; 6; 30; 6; 6; 8; 6; 8; 6; 30; 6; 6; 6; 30; 8; 6; 6; 6; 6; 6; 6; 30; 6; 6; 6; 6; 8; 8; 6; 8; 6; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_C]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Calcium [CS], Cations, Divalent [CS], Cations, Divalent [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Milk Proteins [CS], Nitrogen Binding Agent [EPC], Non-Standardized Food Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC] 

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This page was last updated on: 5/9/2025

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