17089-463 NDC - GUNA ARTHRO RELIEF (ARTERIA SUIS - ALPHA KETOGLUTARICUM ACIDUM - ALPHA LIPOICUM ACIDUM - ASCORBICUM ACIDUM - BARIUM OXALSUCCINICUM - BRYONIA ALBA - CALCAREA CARBONICA - CARTILAGO SUIS - CHLORINUM - CIMICIFUGA RACEMOSA - COLCHICUM AUTUMNALE - DULCAMARA - EMBRYO SUIS - FUNICULUS UMBILICALIS SUIS - GLANDULA SUPRARENALIS SUIS - NADIDUM - NATRUM OXALACETICUM - NATRUM SULPHURICUM - PLACENTA TOTALIS SUIS - RHUS TOXICODENDRON - SULPHUR- VENA SUIS -)

Drug Information

  • Product NDC: 17089-463
  • Proprietary Name: GUNA ARTHRO RELIEF
  • Non Proprietary Name: arteria suis - alpha ketoglutaricum acidum - alpha lipoicum acidum - ascorbicum acidum - barium oxalsuccinicum - bryonia alba - calcarea carbonica - cartilago suis - chlorinum - cimicifuga racemosa - colchicum autumnale - dulcamara - embryo suis - funiculus umbilicalis suis - glandula suprarenalis suis - nadidum - natrum oxalaceticum - natrum sulphuricum - placenta totalis suis - rhus toxicodendron - sulphur- vena suis -
  • Active Ingredient(s): 3 [hp_X]/30mL .ALPHA.-KETOGLUTARIC ACID; 8 [hp_X]/30mL .ALPHA.-LIPOIC ACID; 3 [hp_X]/30mL ASCORBIC ACID; 6 [hp_X]/30mL BARIUM OXALOSUCCINATE; 6 [hp_X]/30mL BLACK COHOSH; 6 [hp_X]/30mL BRYONIA ALBA ROOT; 6 [hp_X]/30mL CHLORINE; 6 [hp_X]/30mL COLCHICUM AUTUMNALE BULB; 3 [hp_X]/30mL NADIDE; 4 [hp_X]/30mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 3 [hp_X]/30mL SODIUM DIETHYL OXALACETATE; 8 [hp_X]/30mL SODIUM SULFATE; 6 [hp_X]/30mL SOLANUM DULCAMARA FLOWER; 4 [hp_X]/30mL SULFUR; 6 [hp_X]/30mL SUS SCROFA ADRENAL GLAND; 6 [hp_X]/30mL SUS SCROFA ARTERY; 6 [hp_X]/30mL SUS SCROFA CARTILAGE; 6 [hp_X]/30mL SUS SCROFA EMBRYO; 6 [hp_X]/30mL SUS SCROFA PLACENTA; 6 [hp_X]/30mL SUS SCROFA UMBILICAL CORD; 6 [hp_X]/30mL SUS SCROFA VEIN; 6 [hp_X]/30mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Ascorbic Acid [CS]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; 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:9/24/2020

Package Information

No. Package Code Package Description Billing Unit
117089-463-181 BOTTLE, DROPPER in 1 BOX (17089-463-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-463The 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 ARTHRO 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 NAMEarteria suis - alpha ketoglutaricum acidum - alpha lipoicum acidum - ascorbicum acidum - barium oxalsuccinicum - bryonia alba - calcarea carbonica - cartilago suis - chlorinum - cimicifuga racemosa - colchicum autumnale - dulcamara - embryo suis - funiculus umbilicalis suis - glandula suprarenalis suis - nadidum - natrum oxalaceticum - natrum sulphuricum - placenta totalis suis - rhus toxicodendron - sulphur- vena suis -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 NAME.ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BLACK COHOSH; BRYONIA ALBA ROOT; CHLORINE; COLCHICUM AUTUMNALE BULB; NADIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM DIETHYL OXALACETATE; SODIUM SULFATE; SOLANUM DULCAMARA FLOWER; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA ARTERY; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; 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 STRENGTH3; 8; 3; 6; 6; 6; 6; 6; 3; 4; 3; 8; 6; 4; 6; 6; 6; 6; 6; 6; 6; 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_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 CLASSESAscorbic Acid [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Vitamin C [EPC] 

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This page was last updated on: 8/8/2025

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