17089-418 NDC - GUNA-ALLERGY T (AMMONIUM CARBONATE - APIS MELLIFERA - ARSENIC TRIOXIDE - BLATTA ORIENTALIS - CUPRIC ACETATE - DRIMIA MARITIMA BULB - EPINEPHRINE - GALPHIMIA GLAUCA FLOWERING TOP - HISTAMINE DIHYDROCHLORIDE - LUFFA OPERCULATA - MANGANESE GLUCONATE - ONION - SCHOENOCAULON OFFICINALE SEED - SODIUM CHLORIDE - SUS SCROFA ADRENAL GLAND - SUS SCROFA BRONCHUS - SUS SCROFA NASAL MUCOSA -)

Drug Information

  • Product NDC: 17089-418
  • Proprietary Name: GUNA-ALLERGY T
  • Non Proprietary Name: ammonium carbonate - apis mellifera - arsenic trioxide - blatta orientalis - cupric acetate - drimia maritima bulb - epinephrine - galphimia glauca flowering top - histamine dihydrochloride - luffa operculata - manganese gluconate - onion - schoenocaulon officinale seed - sodium chloride - sus scrofa adrenal gland - sus scrofa bronchus - sus scrofa nasal mucosa -
  • Active Ingredient(s): 30 [hp_X]/30mL AMMONIUM CARBONATE; 200 [hp_X]/30mL APIS MELLIFERA; 30 [hp_X]/30mL ARSENIC TRIOXIDE; 12 [hp_X]/30mL BLATTA ORIENTALIS; 30 [hp_X]/30mL CUPRIC ACETATE; 30 [hp_X]/30mL DRIMIA MARITIMA BULB; 6 [hp_X]/30mL EPINEPHRINE; 12 [hp_X]/30mL GALPHIMIA GLAUCA FLOWERING TOP; 200 [hp_X]/30mL HISTAMINE DIHYDROCHLORIDE; 12 [hp_X]/30mL LUFFA OPERCULATA FRUIT; 4 [hp_X]/30mL MANGANESE GLUCONATE; 30 [hp_X]/30mL ONION; 30 [hp_X]/30mL SCHOENOCAULON OFFICINALE SEED; 30 [hp_X]/30mL SODIUM CHLORIDE; 12 [hp_X]/30mL SUS SCROFA ADRENAL GLAND; 200 [hp_X]/30mL SUS SCROFA BRONCHUS; 200 [hp_X]/30mL SUS SCROFA NASAL MUCOSA
  • Administration Route(s): ORAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Catecholamine [EPC]; Catecholamines [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]; Insect Proteins [CS]; Magnetic Resonance Contrast Activity [MoA]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Insect Allergenic Extract [EPC]; Paramagnetic Contrast Agent [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

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:5/27/2010

Package Information

No. Package Code Package Description Billing Unit
117089-418-181 BOTTLE, DROPPER in 1 BOX (17089-418-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-418The 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-ALLERGY TThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEammonium carbonate - apis mellifera - arsenic trioxide - blatta orientalis - cupric acetate - drimia maritima bulb - epinephrine - galphimia glauca flowering top - histamine dihydrochloride - luffa operculata - manganese gluconate - onion - schoenocaulon officinale seed - sodium chloride - sus scrofa adrenal gland - sus scrofa bronchus - sus scrofa nasal mucosa -The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe 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 DATE5/27/2010This 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 NAMEAMMONIUM CARBONATE; APIS MELLIFERA; ARSENIC TRIOXIDE; BLATTA ORIENTALIS; CUPRIC ACETATE; DRIMIA MARITIMA BULB; EPINEPHRINE; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; MANGANESE GLUCONATE; ONION; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; SUS SCROFA ADRENAL GLAND; SUS SCROFA BRONCHUS; SUS SCROFA NASAL MUCOSAAn 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 STRENGTH30; 200; 30; 12; 30; 30; 6; 12; 200; 12; 4; 30; 30; 30; 12; 200; 200 
ACTIVE INGRED UNIT[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Catecholamine [EPC], Catecholamines [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], Insect Proteins [CS], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Insect Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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

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