43742-2551 NDC - GLP-4TE HOMO (AACG-A, AACG-B, ADENOSINUM CYCLOPHOSPHORICUM, BERBERINUM, CALCAREA CARBONICA, CINCHONA OFFICINALIS, CHOLINUM, COLIBACILLINUM CUM NATRUM MURIATICUM, CURCUMA LONGA, METHYLCOBALAMIN, DNA, FERRUM METALLICUM, PANAX GINSENG, L-GLUTAMIC ACID, HEPAR SUIS, HYPOTHALAMUS SUIS, INDOLUM, INSULINUM (HUMAN), IODIUM, LYCOPODIUM CLAVATUM, MAGNESIA CARBONICA, L-METHIONINE, PANCREAS SUIS, STOMACH (SUIS), ZINCUM METALLICUM, 7-OXO-DEHYDROEPIANDROSTERONE-3B-ACETATE)

Drug Information

  • Product NDC: 43742-2551
  • Proprietary Name: GLP-4TE HOMO
  • Non Proprietary Name: AACG-A, AACG-B, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, DNA, Ferrum Metallicum, Panax Ginseng, L-Glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum (Human), Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-Methionine, Pancreas Suis, Stomach (Suis), Zincum Metallicum, 7-oxo-Dehydroepiandrosterone-3B-Acetate
  • Active Ingredient(s): 9 [hp_X]/mL APC-356433; 9 [hp_X]/mL APC-356434; 9 [hp_X]/mL ADENOSINE CYCLIC PHOSPHATE; 9 [hp_X]/mL BERBERINE CHLORIDE; 9 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 9 [hp_X]/mL CINCHONA OFFICINALIS BARK; 9 [hp_X]/mL CHOLINE HYDROXIDE; 9 [hp_X]/mL ESCHERICHIA COLI; 9 [hp_X]/mL TURMERIC; 9 [hp_X]/mL METHYLCOBALAMIN; 9 [hp_X]/mL HERRING SPERM DNA; 9 [hp_X]/mL IRON; 9 [hp_X]/mL ASIAN GINSENG; 9 [hp_X]/mL GLUTAMIC ACID; 9 [hp_X]/mL PORK LIVER; 9 [hp_X]/mL SUS SCROFA HYPOTHALAMUS; 9 [hp_X]/mL INDOLE; 9 [hp_X]/mL INSULIN HUMAN; 9 [hp_X]/mL IODINE; 9 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 9 [hp_X]/mL MAGNESIUM CARBONATE; 9 [hp_X]/mL METHIONINE; 9 [hp_X]/mL SUS SCROFA PANCREAS; 9 [hp_X]/mL SUS SCROFA STOMACH; 9 [hp_X]/mL ZINC; 9 [hp_X]/mL 7-KETO-DEHYDROEPIANDROSTERONE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Insulin [CS]; Insulin [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:7/24/2026

Package Information

No. Package Code Package Description Billing Unit

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2551The 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 NAMEGLP-4TE HOMOThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAACG-A, AACG-B, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, DNA, Ferrum Metallicum, Panax Ginseng, L-Glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum (Human), Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-Methionine, Pancreas Suis, Stomach (Suis), Zincum Metallicum, 7-oxo-Dehydroepiandrosterone-3B-AcetateThe 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 DATE7/24/2026This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NAMEAPC-356433; APC-356434; ADENOSINE CYCLIC PHOSPHATE; BERBERINE CHLORIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CINCHONA OFFICINALIS BARK; CHOLINE HYDROXIDE; ESCHERICHIA COLI; TURMERIC; METHYLCOBALAMIN; HERRING SPERM DNA; IRON; ASIAN GINSENG; GLUTAMIC ACID; PORK LIVER; SUS SCROFA HYPOTHALAMUS; INDOLE; INSULIN HUMAN; IODINE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CARBONATE; METHIONINE; SUS SCROFA PANCREAS; SUS SCROFA STOMACH; ZINC; 7-KETO-DEHYDROEPIANDROSTERONEAn 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 STRENGTH9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9; 9 
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_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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESInsulin [CS], Insulin [EPC] 

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This page was last updated on: 8/8/2026

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