17312-420 NDC - NATURAL EYES ALLERGY EYE RELIEF (ALLIUM CEPA, APIS MELLIFICA, EUPHRASIA OFFICINALIS, HISTAMINE HYDROCHLORICUM, PULSATILLA, SABADILLA, SULPHUR)

Drug Information

  • Product NDC: 17312-420
  • Proprietary Name: Natural Eyes Allergy Eye Relief
  • Non Proprietary Name: Allium cepa, Apis mellifica, Euphrasia officinalis, Histamine hydrochloricum, Pulsatilla, Sabadilla, Sulphur
  • Active Ingredient(s): 3 [hp_X]/1 APIS MELLIFERA; 3 [hp_X]/1 EUPHRASIA STRICTA; 9 [hp_X]/1 HISTAMINE DIHYDROCHLORIDE; 3 [hp_X]/1 ONION; 4 [hp_X]/1 PULSATILLA ALPINA WHOLE; 3 [hp_X]/1 SCHOENOCAULON OFFICINALE SEED; 9 [hp_X]/1 SULFUR
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET, ORALLY DISINTEGRATING
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: TRP Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/16/2025

Package Information

No. Package Code Package Description Billing Unit
117312-420-142 BLISTER PACK in 1 PACKAGE (17312-420-14) / 24 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC17312-420The 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 NAMENatural Eyes Allergy Eye ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXFast Dissolving TablesA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEAllium cepa, Apis mellifica, Euphrasia officinalis, Histamine hydrochloricum, Pulsatilla, Sabadilla, SulphurThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, ORALLY DISINTEGRATINGThe 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 DATE3/16/2025This 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 NAMETRP CompanyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAPIS MELLIFERA; EUPHRASIA STRICTA; HISTAMINE DIHYDROCHLORIDE; ONION; PULSATILLA ALPINA WHOLE; SCHOENOCAULON OFFICINALE SEED; SULFURAn 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 STRENGTH3; 3; 9; 3; 4; 3; 9 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 
PHARM CLASSESAllergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS] 

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This page was last updated on: 7/4/2025

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