Guna Deep Cleanse Solution/ Drops
NDC 17089-466

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 17089-466?
  4. Guna Deep Cleanse Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Guna Deep Cleanse (apis mellifera - berberis vulgaris root bark - chelidonium majus - chondrodendron tomentosum root - equisetum hyemale whole - fucus vesiculosus - galium aparine whole - hamamelis virginiana root bark - lycopodium clavatum spore - myosotis arvensis - podophyllum peltatum root - rancid beef - sodium sulfate - solidago virgaurea flowering top - strychnos nux vomica seed - thuja occidentalis leafy twig -) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Guna Spa. This medication is typically used as a allergens [cs]. It is supplied as a solution/ drops for oral administration. This product entry covers the primary NDC 17089-466 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
17089-466
Proprietary Name:
Guna Deep Cleanse
Non-Proprietary Name: [1]
Apis Mellifera - Berberis Vulgaris Root Bark - Chelidonium Majus - Chondrodendron Tomentosum Root - Equisetum Hyemale Whole - Fucus Vesiculosus - Galium Aparine Whole - Hamamelis Virginiana Root Bark - Lycopodium Clavatum Spore - Myosotis Arvensis - Podophyllum Peltatum Root - Rancid Beef - Sodium Sulfate - Solidago Virgaurea Flowering Top - Strychnos Nux Vomica Seed - Thuja Occidentalis Leafy Twig -
Substance Name: [2]
Apis Mellifera; Berberis Vulgaris Root Bark; Chelidonium Majus Root; Chondrodendron Tomentosum Root; Equisetum Hyemale Whole; Fucus Vesiculosus; Galium Aparine Whole; Hamamelis Virginiana Root Bark/stem Bark; Lycopodium Clavatum Spore; Myosotis Arvensis; Podophyllum Peltatum Root; Rancid Beef; Sodium Sulfate; Solidago Virgaurea Flowering Top; Strychnos Nux-vomica Seed; Thuja Occidentalis Leafy Twig
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Guna Spa
Labeler Code:
17089
Product Label ID:
af5e3933-4b2f-0966-e053-2995a90aaf2c
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-24-2020
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 17089-466?

The NDC code 17089-466 is assigned by the FDA to the product Guna Deep Cleanse. It is commonly known by its generic name, apis mellifera - berberis vulgaris root bark - chelidonium majus - chondrodendron tomentosum root - equisetum hyemale whole - fucus vesiculosus - galium aparine whole - hamamelis virginiana root bark - lycopodium clavatum spore - myosotis arvensis - podophyllum peltatum root - rancid beef - sodium sulfate - solidago virgaurea flowering top - strychnos nux vomica seed - thuja occidentalis leafy twig -. This pharmaceutical product is labeled by Guna Spa and is currently categorized as listed product. The medication is a solution/ drops administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 17089-466-18. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Take 15 minutes before meals

What are Active Ingredients of this product?

An 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.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N)
  • CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
  • FUCUS VESICULOSUS (UNII: 535G2ABX9M)
  • FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
  • GALIUM APARINE WHOLE (UNII: Z4B6561488)
  • GALIUM APARINE WHOLE (UNII: Z4B6561488) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • MYOSOTIS ARVENSIS (UNII: C73BK97H5J)
  • MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • PODOPHYLLUM PELTATUM ROOT (UNII: 2S713A4VP3)
  • PODOPHYLLUM PELTATUM ROOT (UNII: 2S713A4VP3) (Active Moiety)
  • CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z)
  • CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z) (Active Moiety)
  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25)
  • EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
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.
What is the Substance Name? An 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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".