43742-2083 NDC - EYE SUPPORT (ALLIUM CEPA, SYMPHYTUM OFFICINALE, ARGENTUM NITRICUM, EYE (SUIS), VACCINIUM MYRTILLUS, APIS MELLIFICA, CALCAREA FLUORICA, CARBONEUM SULPHURATUM, CEDRON, GELSEMIUM SEMPERVIRENS, KALI IODATUM, NUX MOSCHATA, PHOSPHORUS, PHYSOSTIGMA VENENOSUM, STAPHYSAGRIA)

Drug Information

  • Product NDC: 43742-2083
  • Proprietary Name: Eye Support
  • Non Proprietary Name: Allium Cepa, Symphytum Officinale, Argentum Nitricum, Eye (Suis), Vaccinium Myrtillus, Apis Mellifica, Calcarea Fluorica, Carboneum Sulphuratum, Cedron, Gelsemium Sempervirens, Kali Iodatum, Nux Moschata, Phosphorus, Physostigma Venenosum, Staphysagria
  • Active Ingredient(s): 12 [hp_X]/mL APIS MELLIFERA; 6 [hp_X]/mL BILBERRY; 12 [hp_X]/mL CALCIUM FLUORIDE; 12 [hp_X]/mL CARBON DISULFIDE; 6 [hp_X]/mL COMFREY ROOT; 12 [hp_X]/mL DELPHINIUM STAPHISAGRIA SEED; 12 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT; 12 [hp_X]/mL HOMALOLEPIS CEDRON SEED; 12 [hp_X]/mL NUTMEG; 6 [hp_X]/mL ONION; 12 [hp_X]/mL PHOSPHORUS; 12 [hp_X]/mL PHYSOSTIGMA VENENOSUM SEED; 12 [hp_X]/mL POTASSIUM IODIDE; 6 [hp_X]/mL SILVER NITRATE; 6 [hp_X]/mL SUS SCROFA EYE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Food Additives [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]

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:5/9/2023

Package Information

No. Package Code Package Description Billing Unit
143742-2083-130 mL in 1 BOTTLE, DROPPER (43742-2083-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2083The 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 NAMEEye 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 NAMEAllium Cepa, Symphytum Officinale, Argentum Nitricum, Eye (Suis), Vaccinium Myrtillus, Apis Mellifica, Calcarea Fluorica, Carboneum Sulphuratum, Cedron, Gelsemium Sempervirens, Kali Iodatum, Nux Moschata, Phosphorus, Physostigma Venenosum, StaphysagriaThe 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 DATE5/9/2023This 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 NAMEAPIS MELLIFERA; BILBERRY; CALCIUM FLUORIDE; CARBON DISULFIDE; COMFREY ROOT; DELPHINIUM STAPHISAGRIA SEED; GELSEMIUM SEMPERVIRENS ROOT; HOMALOLEPIS CEDRON SEED; NUTMEG; ONION; PHOSPHORUS; PHYSOSTIGMA VENENOSUM SEED; POTASSIUM IODIDE; SILVER NITRATE; SUS SCROFA EYEAn 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; 6; 12; 12; 6; 12; 12; 12; 12; 6; 12; 12; 12; 6; 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 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS] 

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This page was last updated on: 7/25/2025

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