17089-465 NDC - GUNA PAIN MANAGEMENT (ACHILLEA MILLEFOLIUM WHOLE - BELLIS PERENNIS WHOLE - MATRICARIA CHAMOMILLA WHOLE - TOXICODENDRON PUBESCENS WHOLE - RUTA GRAVEOLENS FLOWERING TOP - COMFREY ROOT - APIS MELLIFERA - BRYONIA ALBA ROOT - HISTAMINE HYDROCHLORIDE - HYPERICUM PERFORATUM - KALMIA LATIFOLIA LEAF - ARNICA MONTANA WHOLE - PORK LIVER -)

Drug Information

  • Product NDC: 17089-465
  • Proprietary Name: GUNA PAIN MANAGEMENT
  • Non Proprietary Name: achillea millefolium whole - bellis perennis whole - matricaria chamomilla whole - toxicodendron pubescens whole - ruta graveolens flowering top - comfrey root - apis mellifera - bryonia alba root - histamine hydrochloride - hypericum perforatum - kalmia latifolia leaf - arnica montana whole - pork liver -
  • Active Ingredient(s): 2 [hp_X]/30mL ACHILLEA MILLEFOLIUM WHOLE; 30 [hp_X]/30mL APIS MELLIFERA; 3 [hp_X]/30mL ARNICA MONTANA WHOLE; 2 [hp_X]/30mL BELLIS PERENNIS WHOLE; 6 [hp_X]/30mL BRYONIA ALBA ROOT; 6 [hp_X]/30mL COMFREY ROOT; 12 [hp_X]/30mL HISTAMINE DIHYDROCHLORIDE; 3 [hp_X]/30mL HYPERICUM PERFORATUM; 6 [hp_X]/30mL KALMIA LATIFOLIA LEAF; 2 [hp_X]/30mL MATRICARIA CHAMOMILLA WHOLE; 6 [hp_X]/30mL PORK LIVER; 4 [hp_X]/30mL RUTA GRAVEOLENS FLOWERING TOP; 8 [hp_X]/30mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Standardized Insect Venom Allergenic Extract [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:9/24/2020

Package Information

No. Package Code Package Description Billing Unit
117089-465-181 BOTTLE, DROPPER in 1 BOX (17089-465-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-465The 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 PAIN MANAGEMENTThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEachillea millefolium whole - bellis perennis whole - matricaria chamomilla whole - toxicodendron pubescens whole - ruta graveolens flowering top - comfrey root - apis mellifera - bryonia alba root - histamine hydrochloride - hypericum perforatum - kalmia latifolia leaf - arnica montana whole - pork liver -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 DATE9/24/2020This 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 NAMEACHILLEA MILLEFOLIUM WHOLE; APIS MELLIFERA; ARNICA MONTANA WHOLE; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; COMFREY ROOT; HISTAMINE DIHYDROCHLORIDE; HYPERICUM PERFORATUM; KALMIA LATIFOLIA LEAF; MATRICARIA CHAMOMILLA WHOLE; PORK LIVER; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS 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 STRENGTH2; 30; 3; 2; 6; 6; 12; 3; 6; 2; 6; 4; 8 
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 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] 

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This page was last updated on: 2/5/2026

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