17089-464 NDC - GUNA FLAM RELIEF (ACONITUM NAPELLUS - APIS MELLIFERA - ARNICA MONTANA WHOLE - ATROPA BELLADONNA - BASIC CUPRIC CARBONATE - BRYONIA ALBA ROOT - MATRICARIA CHAMOMILLA WHOLE - CALCIUM SULFIDE - CITRIC ACID MONOHYDRATE - ECHINACEA ANGUSTIFOLIA - FERRIC PHOSPHATE - PHYTOLACCA AMERICANA ROOT - RANCID BEEF - SODIUM PYRUVATE - PORK LIVER - RANCID BEEF - SUS SCROFA PITUITARY GLAND -)

Drug Information

  • Product NDC: 17089-464
  • Proprietary Name: GUNA FLAM RELIEF
  • Non Proprietary Name: ACONITUM NAPELLUS - APIS MELLIFERA - ARNICA MONTANA WHOLE - ATROPA BELLADONNA - BASIC CUPRIC CARBONATE - BRYONIA ALBA ROOT - MATRICARIA CHAMOMILLA WHOLE - CALCIUM SULFIDE - CITRIC ACID MONOHYDRATE - ECHINACEA ANGUSTIFOLIA - FERRIC PHOSPHATE - PHYTOLACCA AMERICANA ROOT - RANCID BEEF - SODIUM PYRUVATE - PORK LIVER - RANCID BEEF - SUS SCROFA PITUITARY GLAND -
  • Active Ingredient(s): 6 [hp_X]/30mL ACONITUM NAPELLUS WHOLE; 6 [hp_X]/30mL APIS MELLIFERA; 3 [hp_X]/30mL ARNICA MONTANA; 6 [hp_X]/30mL ATROPA BELLADONNA; 4 [hp_X]/30mL BASIC CUPRIC CARBONATE; 6 [hp_X]/30mL BRYONIA ALBA ROOT; 6 [hp_X]/30mL CALCIUM SULFIDE; 3 [hp_X]/30mL CITRIC ACID MONOHYDRATE; 4 [hp_X]/30mL ECHINACEA ANGUSTIFOLIA WHOLE; 12 [hp_X]/30mL FERRIC PHOSPHATE; 2 [hp_X]/30mL MATRICARIA CHAMOMILLA WHOLE; 6 [hp_X]/30mL PHYTOLACCA AMERICANA ROOT; 6 [hp_X]/30mL PORK LIVER; 30 [hp_X]/30mL RANCID BEEF; 3 [hp_X]/30mL SODIUM PYRUVATE; 200 [hp_X]/30mL SUS SCROFA PITUITARY GLAND
  • Administration Route(s): ORAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Acidifying Activity [MoA]; Allergens [CS]; Anti-coagulant [EPC]; Bee Venoms [CS]; Calcium Chelating Activity [MoA]; Calculi Dissolution Agent [EPC]; Cell-mediated Immunity [PE]; Decreased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Iron [CS]; Parenteral Iron Replacement [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; 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
117089-464-181 BOTTLE, DROPPER in 1 BOX (17089-464-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-464The 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 FLAM 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 NAMEACONITUM NAPELLUS - APIS MELLIFERA - ARNICA MONTANA WHOLE - ATROPA BELLADONNA - BASIC CUPRIC CARBONATE - BRYONIA ALBA ROOT - MATRICARIA CHAMOMILLA WHOLE - CALCIUM SULFIDE - CITRIC ACID MONOHYDRATE - ECHINACEA ANGUSTIFOLIA - FERRIC PHOSPHATE - PHYTOLACCA AMERICANA ROOT - RANCID BEEF - SODIUM PYRUVATE - PORK LIVER - RANCID BEEF - SUS SCROFA PITUITARY GLAND -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 NAMEACONITUM NAPELLUS WHOLE; APIS MELLIFERA; ARNICA MONTANA; ATROPA BELLADONNA; BASIC CUPRIC CARBONATE; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CITRIC ACID MONOHYDRATE; ECHINACEA ANGUSTIFOLIA WHOLE; FERRIC PHOSPHATE; MATRICARIA CHAMOMILLA WHOLE; PHYTOLACCA AMERICANA ROOT; PORK LIVER; RANCID BEEF; SODIUM PYRUVATE; SUS SCROFA PITUITARY GLANDAn 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; 3; 6; 4; 6; 6; 3; 4; 12; 2; 6; 6; 30; 3; 200 
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 
PHARM CLASSESAcidifying Activity [MoA], Allergens [CS], Anti-coagulant [EPC], Bee Venoms [CS], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Decreased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Standardized Insect Venom Allergenic Extract [EPC] 

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

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