NDC 17089-474 Guna Kidney Plus

Calcium Sulfide - Chondrodendron Tomentosum Root - Equisetum Hyemale - Sus Scrofa Pituitary Gland - Apis Mellifera - Urtica Urens - Sodium Chloride - Lobaria Pulmonaria - Horse Chestnut - Berberis Vulgaris Fruit - Solidago Viragaurea Flowering Top -

NDC Product Code 17089-474

NDC CODE: 17089-474

Proprietary Name: Guna Kidney Plus What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Calcium Sulfide - Chondrodendron Tomentosum Root - Equisetum Hyemale - Sus Scrofa Pituitary Gland - Apis Mellifera - Urtica Urens - Sodium Chloride - Lobaria Pulmonaria - Horse Chestnut - Berberis Vulgaris Fruit - Solidago Viragaurea Flowering Top - What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.

NDC Code Structure

  • 17089 - Guna Spa

NDC 17089-474-18

Package Description: 1 BOTTLE, DROPPER in 1 BOX > 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Guna Kidney Plus with NDC 17089-474 is a a human over the counter drug product labeled by Guna Spa. The generic name of Guna Kidney Plus is calcium sulfide - chondrodendron tomentosum root - equisetum hyemale - sus scrofa pituitary gland - apis mellifera - urtica urens - sodium chloride - lobaria pulmonaria - horse chestnut - berberis vulgaris fruit - solidago viragaurea flowering top -. The product's dosage form is solution/ drops and is administered via oral form.

Labeler Name: Guna Spa

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Guna Kidney Plus Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CALCIUM SULFIDE 6 [hp_X]/30mL
  • APIS MELLIFERA 12 [hp_X]/30mL
  • SODIUM CHLORIDE 10 [hp_X]/30mL
  • HORSE CHESTNUT 2 [hp_X]/30mL
  • URTICA URENS 6 [hp_X]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Guna Spa
Labeler Code: 17089
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 01-17-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Guna Kidney Plus Product Label Images

Guna Kidney Plus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

Take 15 minutes before meals

Inactive Ingredient

Inactive Ingredient: Ethyl alcohol 30%.


Questions?: info@gunainc.com, tel. (484) 223-3500


Adults and children 12 years and older 20 drops in a little water, 2 times per day

Children between 12 and 6 years of age 10 drops in a little water, 2 times per day

Children under 6 years consult a physician


Keep out of reach of children

Stop use and ask doctor if symptoms persist more than 5 days.

If pregnant or breast-feeding ask a health professional before use.

Keep out of reach of children. In case of overdose, get professional assistance or contact a Poison Control Center immediately

Contains ethyl alcohol 30%


If pregnant or breast-feeding ask a health care professional before use


  • Supports kidney and bladder function, relieves urinary discomfort

Active Ingredients/Purpose

Equisetum hyemale 3X Supports kidney and bladder functionApis mellifica 12X Relieves inflammationHypophysys suis 200X Supports endocrine functionNatrum muriaticum 10X Relieves urinary discomfort, urgency to urinateSticta pulmonaria 6X Relieves urinary discomfort, urgency to urinateAesculus hippocastanum 2X Relieves urinary discomfort, urgency to urinateBerberis vulgaris 3X Supports kidney functionPareira brava 4X Relieves urinary discomfortSolidago virgaurea 2X Supports kidney and bladder functionUrtica urens 6X Supports kidney functionHepar sulphuris calcareum 6X Relieves urinary discomfort

* Please review the disclaimer below.