17089-306 NDC - GUNA-DIZZY (.ALPHA.-KETOGLUTARIC ACID - AMBERGRIS - ANAMIRTA COCCULUS SEED - CONIUM MACULATUM FLOWERING TOP - EPINEPHRINE - FUMARIC ACID - MALIC ACID - MELATONIN - MINERAL OIL - PTERIDIUM AQUILINUM ROOT - PYRIDOXINE HYDROCHLORIDE - QUINHYDRONE - QUININE - SUS SCROFA ARTERY - SUS SCROFA CEREBELLUM - SUS SCROFA PLACENTA - THIAMINE HYDROCHLORIDE - TOBACCO LEAF -)

Drug Information

  • Product NDC: 17089-306
  • Proprietary Name: GUNA-DIZZY
  • Non Proprietary Name: .alpha.-ketoglutaric acid - ambergris - anamirta cocculus seed - conium maculatum flowering top - epinephrine - fumaric acid - malic acid - melatonin - mineral oil - pteridium aquilinum root - pyridoxine hydrochloride - quinhydrone - quinine - sus scrofa artery - sus scrofa cerebellum - sus scrofa placenta - thiamine hydrochloride - tobacco leaf -
  • Active Ingredient(s): 6 [hp_X]/30mL .ALPHA.-KETOGLUTARIC ACID; 6 [hp_X]/30mL AMBERGRIS; 4 [hp_X]/30mL ANAMIRTA COCCULUS SEED; 3 [hp_X]/30mL CONIUM MACULATUM FLOWERING TOP; 6 [hp_X]/30mL EPINEPHRINE; 6 [hp_X]/30mL FUMARIC ACID; 6 [hp_X]/30mL MALIC ACID; 4 [hp_C]/30mL MELATONIN; 8 [hp_X]/30mL MINERAL OIL; 8 [hp_X]/30mL PTERIDIUM AQUILINUM ROOT; 6 [hp_X]/30mL PYRIDOXINE HYDROCHLORIDE; 6 [hp_X]/30mL QUINHYDRONE; 6 [hp_X]/30mL QUININE SALICYLATE; 6 [hp_X]/30mL SUS SCROFA ARTERY; 6 [hp_X]/30mL SUS SCROFA CEREBELLUM; 6 [hp_X]/30mL SUS SCROFA PLACENTA; 4 [hp_X]/30mL THIAMINE HYDROCHLORIDE; 6 [hp_X]/30mL TOBACCO LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Analogs/Derivatives [Chemical/Ingredient]; Antimalarial [EPC]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Depigmenting Activity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Melanin Synthesis Inhibitor [EPC]; Melanin Synthesis Inhibitors [MoA]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B6 Analog [EPC]; 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:5/23/2006

Package Information

No. Package Code Package Description Billing Unit
117089-306-181 BOTTLE, DROPPER in 1 BOX (17089-306-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-306The 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-DIZZYThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME.alpha.-ketoglutaric acid - ambergris - anamirta cocculus seed - conium maculatum flowering top - epinephrine - fumaric acid - malic acid - melatonin - mineral oil - pteridium aquilinum root - pyridoxine hydrochloride - quinhydrone - quinine - sus scrofa artery - sus scrofa cerebellum - sus scrofa placenta - thiamine hydrochloride - tobacco leaf -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 DATE5/23/2006This 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 NAME.ALPHA.-KETOGLUTARIC ACID; AMBERGRIS; ANAMIRTA COCCULUS SEED; CONIUM MACULATUM FLOWERING TOP; EPINEPHRINE; FUMARIC ACID; MALIC ACID; MELATONIN; MINERAL OIL; PTERIDIUM AQUILINUM ROOT; PYRIDOXINE HYDROCHLORIDE; QUINHYDRONE; QUININE SALICYLATE; SUS SCROFA ARTERY; SUS SCROFA CEREBELLUM; SUS SCROFA PLACENTA; THIAMINE HYDROCHLORIDE; TOBACCO LEAFAn 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 STRENGTH6; 6; 4; 3; 6; 6; 6; 4; 8; 8; 6; 6; 6; 6; 6; 6; 4; 6 
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_C]/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], Analogs/Derivatives [Chemical/Ingredient], Antimalarial [EPC], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Depigmenting Activity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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

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