17089-476 NDC - GUNA HAY FEVER RELIEF (STRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -)

Drug Information

  • Product NDC: 17089-476
  • Proprietary Name: GUNA HAY FEVER RELIEF
  • Non Proprietary Name: strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -
  • Active Ingredient(s): 200 [hp_X]/4g APIS MELLIFERA; 30 [hp_X]/4g ARSENIC TRIOXIDE; 5 [hp_X]/4g EUPHRASIA STRICTA; 4 [hp_X]/4g GALPHIMIA GLAUCA FLOWERING TOP; 200 [hp_X]/4g HISTAMINE DIHYDROCHLORIDE; 8 [hp_X]/4g MANGANESE; 30 [hp_X]/4g ONION; 6 [hp_X]/4g SCHOENOCAULON OFFICINALE SEED; 6 [hp_X]/4g SILVER NITRATE; 4 [hp_X]/4g STRYCHNOS NUX-VOMICA SEED; 30 [hp_X]/4g SULFUR
  • Administration Route(s): ORAL
  • Dosage Form(s): PELLET
  • 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]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; 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: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/17/2021

Package Information

No. Package Code Package Description Billing Unit
117089-476-202 TUBE in 1 BOX (17089-476-20) / 4 g in 1 TUBE
217089-476-211 TUBE in 1 BOX (17089-476-21) / 4 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-476The 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 NAMEGUNA HAY FEVER RELIEFThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEstrychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPELLETThe 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 DATE2/17/2021This 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 NAMEGuna spaName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAPIS MELLIFERA; ARSENIC TRIOXIDE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; MANGANESE; ONION; SCHOENOCAULON OFFICINALE SEED; SILVER NITRATE; STRYCHNOS NUX-VOMICA 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 STRENGTH200; 30; 5; 4; 200; 8; 30; 6; 6; 4; 30 
ACTIVE INGRED UNIT[hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g 
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], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], 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: 7/4/2025

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