17089-419 NDC - GUNA-RHINO NOSE (APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE -)

Drug Information

  • Product NDC: 17089-419
  • Proprietary Name: GUNA-RHINO NOSE
  • Non Proprietary Name: apis mellifera - aralia racemosa root - ascorbic acid - black currant - copper - euphorbia resinifera resin - european elderberry - helianthemum canadense - histamine dihydrochloride - human interleukin 12 - human interleukin-10 (nonglycosylated) - interferon gamma-1b - manganese gluconate - melilotus - onion - plantago major - rosa canina fruit - silver nitrate -
  • Active Ingredient(s): 12 [hp_X]/30mL APIS MELLIFERA; 1 [hp_X]/30mL ARALIA RACEMOSA ROOT; 2 [hp_X]/30mL ASCORBIC ACID; 1 [hp_X]/30mL BLACK CURRANT; 4 [hp_X]/30mL COPPER; 4 [hp_X]/30mL EUPHORBIA RESINIFERA RESIN; 2 [hp_X]/30mL EUROPEAN ELDERBERRY; 4 [hp_X]/30mL HELIANTHEMUM CANADENSE; 200 [hp_X]/30mL HISTAMINE DIHYDROCHLORIDE; 4 [hp_C]/30mL HUMAN INTERLEUKIN 12; 4 [hp_C]/30mL INTERFERON GAMMA-1B; 4 [hp_C]/30mL INTERLEUKIN-10; 4 [hp_X]/30mL MANGANESE GLUCONATE; 3 [hp_X]/30mL MELILOTUS; 8 [hp_X]/30mL ONION; 2 [hp_X]/30mL PLANTAGO MAJOR; 1 [hp_X]/30mL ROSA CANINA FRUIT; 10 [hp_X]/30mL SILVER NITRATE
  • Administration Route(s): ORAL
  • Dosage Form(s): SPRAY
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Ascorbic Acid [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Inhibit Ovum Fertilization [PE]; Interferon gamma [EPC]; Interferon-gamma [CS]; Magnetic Resonance Contrast Activity [MoA]; Non-Standardized Food Allergenic Extract [EPC]; Paramagnetic Contrast Agent [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]; Vitamin C [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
117089-419-231 BOTTLE, SPRAY in 1 BOX (17089-419-23) / 30 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-419The 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-RHINO NOSEThe 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 mellifera - aralia racemosa root - ascorbic acid - black currant - copper - euphorbia resinifera resin - european elderberry - helianthemum canadense - histamine dihydrochloride - human interleukin 12 - human interleukin-10 (nonglycosylated) - interferon gamma-1b - manganese gluconate - melilotus - onion - plantago major - rosa canina fruit - silver nitrate -The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe 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 NAMEAPIS MELLIFERA; ARALIA RACEMOSA ROOT; ASCORBIC ACID; BLACK CURRANT; COPPER; EUPHORBIA RESINIFERA RESIN; EUROPEAN ELDERBERRY; HELIANTHEMUM CANADENSE; HISTAMINE DIHYDROCHLORIDE; HUMAN INTERLEUKIN 12; INTERFERON GAMMA-1B; INTERLEUKIN-10; MANGANESE GLUCONATE; MELILOTUS; ONION; PLANTAGO MAJOR; ROSA CANINA FRUIT; SILVER NITRATEAn 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; 1; 2; 1; 4; 4; 2; 4; 200; 4; 4; 4; 4; 3; 8; 2; 1; 10 
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_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Ascorbic Acid [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Interferon gamma [EPC], Interferon-gamma [CS], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS], Vitamin C [EPC] 

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

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