17089-472 NDC - GUNA SINUS PLUS (ALTHAEA OFFICINALIS LEAF - CALCIUM SULFIDE - COPPER - DRIMIA MARITIMA BULB - ECHINACEA ANGUSTIFOLIA - HYDRASTIS CANADENSIS WHOLE - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR WHOLE - POTASSIUM DICHROMATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA -)

Drug Information

  • Product NDC: 17089-472
  • Proprietary Name: GUNA SINUS PLUS
  • Non Proprietary Name: ALTHAEA OFFICINALIS LEAF - CALCIUM SULFIDE - COPPER - DRIMIA MARITIMA BULB - ECHINACEA ANGUSTIFOLIA - HYDRASTIS CANADENSIS WHOLE - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR WHOLE - POTASSIUM DICHROMATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA -
  • Active Ingredient(s): 2 [hp_X]/30mL ALTHAEA OFFICINALIS LEAF; 3 [hp_X]/30mL ASCORBIC ACID; 6 [hp_X]/30mL CALCIUM SULFIDE; 8 [hp_X]/30mL COPPER; 12 [hp_X]/30mL DRIMIA MARITIMA BULB; 3 [hp_X]/30mL ECHINACEA ANGUSTIFOLIA; 6 [hp_X]/30mL HYDRASTIS CANADENSIS WHOLE; 2 [hp_X]/30mL LOBARIA PULMONARIA; 8 [hp_X]/30mL MANGANESE; 8 [hp_X]/30mL MERCURIC SULFIDE; 6 [hp_X]/30mL ONION; 2 [hp_X]/30mL PLANTAGO MAJOR WHOLE; 6 [hp_X]/30mL POTASSIUM DICHROMATE; 6 [hp_X]/30mL PULSATILLA VULGARIS; 6 [hp_X]/30mL SILICON DIOXIDE; 10 [hp_X]/30mL SILVER NITRATE; 12 [hp_X]/30mL SINUSITISINUM; 6 [hp_X]/30mL SUS SCROFA NASAL MUCOSA
  • Administration Route(s): NASAL
  • Dosage Form(s): SPRAY
  • Pharmacy Class(es): Allergens [CS]; Ascorbic Acid [CS]; Cell-mediated Immunity [PE]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Inhibit Ovum Fertilization [PE]; Non-Standardized Food Allergenic Extract [EPC]; Vegetable Proteins [CS]; 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:2/17/2021

Package Information

No. Package Code Package Description Billing Unit
117089-472-231 BOTTLE, SPRAY in 1 BOX (17089-472-23) / 30 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-472The 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 SINUS PLUSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEALTHAEA OFFICINALIS LEAF - CALCIUM SULFIDE - COPPER - DRIMIA MARITIMA BULB - ECHINACEA ANGUSTIFOLIA - HYDRASTIS CANADENSIS WHOLE - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR WHOLE - POTASSIUM DICHROMATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA -The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMENASALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/17/2021This 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 NAMEALTHAEA OFFICINALIS LEAF; ASCORBIC ACID; CALCIUM SULFIDE; COPPER; DRIMIA MARITIMA BULB; ECHINACEA ANGUSTIFOLIA; HYDRASTIS CANADENSIS WHOLE; LOBARIA PULMONARIA; MANGANESE; MERCURIC SULFIDE; ONION; PLANTAGO MAJOR WHOLE; POTASSIUM DICHROMATE; PULSATILLA VULGARIS; SILICON DIOXIDE; SILVER NITRATE; SINUSITISINUM; SUS SCROFA NASAL MUCOSAAn 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; 3; 6; 8; 12; 3; 6; 2; 8; 8; 6; 2; 6; 6; 6; 10; 12; 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 
PHARM CLASSESAllergens [CS], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Vegetable Proteins [CS], Vitamin C [EPC] 

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

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