17089-298 NDC - GUNA-KIDNEY (CHONDRODENDRON TOMENTOSUM ROOT - CLERODENDRANTHUS SPICATUS LEAF - EQUISETUM HYEMALE - ESCHERICHIA COLI - HIERACIUM PILOSELLA FLOWERING TOP - METHYLENE BLUE - NITRIC ACID - ONONIS CAMPESTRIS - PLANTAGO MAJOR - PORK KIDNEY - POTASSIUM NITRATE - PROTEUS VULGARIS - QUINHYDRONE - SARSAPARILLA - SOLIDAGO VIRGAUREA FLOWERING TOP - SUCCINIC ACID - SUS SCROFA URETER - SUS SCROFA URINARY BLADDER -)

Drug Information

  • Product NDC: 17089-298
  • Proprietary Name: GUNA-KIDNEY
  • Non Proprietary Name: chondrodendron tomentosum root - clerodendranthus spicatus leaf - equisetum hyemale - escherichia coli - hieracium pilosella flowering top - methylene blue - nitric acid - ononis campestris - plantago major - pork kidney - potassium nitrate - proteus vulgaris - quinhydrone - sarsaparilla - solidago virgaurea flowering top - succinic acid - sus scrofa ureter - sus scrofa urinary bladder -
  • Active Ingredient(s): 2 [hp_X]/30mL CHONDRODENDRON TOMENTOSUM ROOT; 2 [hp_X]/30mL CLERODENDRANTHUS SPICATUS LEAF; 3 [hp_X]/30mL EQUISETUM HYEMALE; 12 [hp_X]/30mL ESCHERICHIA COLI; 1 [hp_X]/30mL HIERACIUM PILOSELLA FLOWERING TOP; 8 [hp_X]/30mL METHYLENE BLUE; 12 [hp_X]/30mL NITRIC ACID; 2 [hp_X]/30mL ONONIS CAMPESTRIS; 2 [hp_X]/30mL PLANTAGO MAJOR; 8 [hp_X]/30mL PORK KIDNEY; 12 [hp_X]/30mL POTASSIUM NITRATE; 12 [hp_X]/30mL PROTEUS VULGARIS; 8 [hp_X]/30mL QUINHYDRONE; 2 [hp_X]/30mL SARSAPARILLA; 1 [hp_X]/30mL SOLIDAGO VIRGAUREA FLOWERING TOP; 6 [hp_X]/30mL SUCCINIC ACID; 8 [hp_X]/30mL SUS SCROFA URETER; 8 [hp_X]/30mL SUS SCROFA URINARY BLADDER
  • Administration Route(s): ORAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Depigmenting Activity [PE]; Melanin Synthesis Inhibitor [EPC]; Melanin Synthesis Inhibitors [MoA]; Oxidation-Reduction Activity [MoA]; Oxidation-Reduction Agent [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
117089-298-181 BOTTLE, DROPPER in 1 BOX (17089-298-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-298The 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-KIDNEYThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEchondrodendron tomentosum root - clerodendranthus spicatus leaf - equisetum hyemale - escherichia coli - hieracium pilosella flowering top - methylene blue - nitric acid - ononis campestris - plantago major - pork kidney - potassium nitrate - proteus vulgaris - quinhydrone - sarsaparilla - solidago virgaurea flowering top - succinic acid - sus scrofa ureter - sus scrofa urinary bladder -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 NAMECHONDRODENDRON TOMENTOSUM ROOT; CLERODENDRANTHUS SPICATUS LEAF; EQUISETUM HYEMALE; ESCHERICHIA COLI; HIERACIUM PILOSELLA FLOWERING TOP; METHYLENE BLUE; NITRIC ACID; ONONIS CAMPESTRIS; PLANTAGO MAJOR; PORK KIDNEY; POTASSIUM NITRATE; PROTEUS VULGARIS; QUINHYDRONE; SARSAPARILLA; SOLIDAGO VIRGAUREA FLOWERING TOP; SUCCINIC ACID; SUS SCROFA URETER; SUS SCROFA URINARY BLADDERAn 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; 2; 3; 12; 1; 8; 12; 2; 2; 8; 12; 12; 8; 2; 1; 6; 8; 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; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL 
PHARM CLASSESDepigmenting Activity [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA], Oxidation-Reduction Activity [MoA], Oxidation-Reduction Agent [EPC] 

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

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