43742-2550 NDC - MCAS SUPPORT (APIS MELLIFICA, ANTIMONIUM CRUDUM, ASCORBICUM ACIDUM, BOVISTA, CARBOLICUM ACIDUM, CHAMOMILLA, CORTISONE ACETICUM, GINKGO BILOBA, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, NATRUM MURIATICUM, QUERCETIN, RHUS TOX, SCUTELLARIA LATERIFLORA, STOMACH (SUIS), URTICA URENS)

Drug Information

  • Product NDC: 43742-2550
  • Proprietary Name: MCAS Support
  • Non Proprietary Name: Apis Mellifica, Antimonium Crudum, Ascorbicum Acidum, Bovista, Carbolicum Acidum, Chamomilla, Cortisone Aceticum, Ginkgo Biloba, Hepar Suis, Histaminum Hydrochloricum, Natrum Muriaticum, Quercetin, Rhus Tox, Scutellaria Lateriflora, Stomach (Suis), Urtica Urens
  • Active Ingredient(s): 12 [hp_X]/mL ANTIMONY TRISULFIDE; 12 [hp_X]/mL APIS MELLIFERA; 6 [hp_X]/mL ASCORBIC ACID; 6 [hp_X]/mL CORTISONE ACETATE; 6 [hp_X]/mL GINKGO; 6 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE; 6 [hp_X]/mL LYCOPERDON UTRIFORME FRUITING BODY; 6 [hp_X]/mL MATRICARIA CHAMOMILLA WHOLE; 12 [hp_X]/mL PHENOL; 8 [hp_X]/mL PORK LIVER; 12 [hp_X]/mL QUERCETIN; 12 [hp_X]/mL SCUTELLARIA LATERIFLORA WHOLE; 6 [hp_X]/mL SODIUM CHLORIDE; 8 [hp_X]/mL SUS SCROFA STOMACH; 12 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF; 6 [hp_X]/mL URTICA URENS WHOLE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Ascorbic Acid [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Standardized Insect Venom Allergenic Extract [EPC]; Vitamin C [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:6/24/2026

Package Information

No. Package Code Package Description Billing Unit

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2550The 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 NAMEMCAS SupportThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEApis Mellifica, Antimonium Crudum, Ascorbicum Acidum, Bovista, Carbolicum Acidum, Chamomilla, Cortisone Aceticum, Ginkgo Biloba, Hepar Suis, Histaminum Hydrochloricum, Natrum Muriaticum, Quercetin, Rhus Tox, Scutellaria Lateriflora, Stomach (Suis), Urtica UrensThe 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 DATE6/24/2026This 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 NAMEANTIMONY TRISULFIDE; APIS MELLIFERA; ASCORBIC ACID; CORTISONE ACETATE; GINKGO; HISTAMINE DIHYDROCHLORIDE; LYCOPERDON UTRIFORME FRUITING BODY; MATRICARIA CHAMOMILLA WHOLE; PHENOL; PORK LIVER; QUERCETIN; SCUTELLARIA LATERIFLORA WHOLE; SODIUM CHLORIDE; SUS SCROFA STOMACH; TOXICODENDRON PUBESCENS LEAF; URTICA URENS WHOLEAn 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 STRENGTH12; 12; 6; 6; 6; 6; 6; 6; 12; 8; 12; 12; 6; 8; 12; 6 
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 
PHARM CLASSESAllergens [CS], Ascorbic Acid [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC], Vitamin C [EPC] 

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This page was last updated on: 7/7/2026

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