NDC 17089-462 Guna Lympho Detox

Aesculus Hippocastanum - Apis Mellifera - Calendula Officinalis Flower - Hexaketocyclohexane - Equisetum Hyemale - Fumaric Acid - Graphite - Hydrastis Canadensis - Hydrocotyle Asiatica - Juglans Regia - Levothyroxine - Magnesium Phosphate - Malic Acid - Myosotis Arvensis - Phytolacca Americana Root - Sarsaparilla - Sodium Diethyl Oxalacetate - Sodium Pyruvate - Sus Scrofa Placenta - Taraxacum Officinale -

NDC Product Code 17089-462

NDC CODE: 17089-462

Proprietary Name: Guna Lympho Detox 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: Aesculus Hippocastanum - Apis Mellifera - Calendula Officinalis Flower - Hexaketocyclohexane - Equisetum Hyemale - Fumaric Acid - Graphite - Hydrastis Canadensis - Hydrocotyle Asiatica - Juglans Regia - Levothyroxine - Magnesium Phosphate - Malic Acid - Myosotis Arvensis - Phytolacca Americana Root - Sarsaparilla - Sodium Diethyl Oxalacetate - Sodium Pyruvate - Sus Scrofa Placenta - Taraxacum Officinale - 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.

NDC Code Structure

  • 17089 - Guna Spa

NDC 17089-462-18

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

NDC Product Information

Guna Lympho Detox with NDC 17089-462 is a a human over the counter drug product labeled by Guna Spa. The generic name of Guna Lympho Detox is aesculus hippocastanum - apis mellifera - calendula officinalis flower - hexaketocyclohexane - equisetum hyemale - fumaric acid - graphite - hydrastis canadensis - hydrocotyle asiatica - juglans regia - levothyroxine - magnesium phosphate - malic acid - myosotis arvensis - phytolacca americana root - sarsaparilla - sodium diethyl oxalacetate - sodium pyruvate - sus scrofa placenta - taraxacum officinale -. 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 Lympho Detox 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.

  • APIS MELLIFERA 8 [hp_X]/30mL
  • CALENDULA OFFICINALIS FLOWER 1 [hp_X]/30mL
  • MALIC ACID 6 [hp_X]/30mL
  • EQUISETUM HYEMALE 3 [hp_X]/30mL
  • FUMARIC ACID 6 [hp_X]/30mL
  • GRAPHITE 12 [hp_X]/30mL
  • JUGLANS REGIA FRUIT RIND, IMMATURE 5 [hp_X]/30mL
  • LEVOTHYROXINE 12 [hp_X]/30mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/30mL
  • MYOSOTIS ARVENSIS 4 [hp_X]/30mL
  • SODIUM DIETHYL OXALACETATE 6 [hp_X]/30mL
  • SODIUM PYRUVATE 6 [hp_X]/30mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/30mL
  • SARSAPARILLA 3 [hp_X]/30mL
  • TARAXACUM OFFICINALE 1 [hp_X]/30mL
  • DODECAHYDROXYCYCLOHEXANE DIHYDRATE 6 [hp_X]/30mL
  • SUS SCROFA PLACENTA 6 [hp_X]/30mL
  • HORSE CHESTNUT 2 [hp_X]/30mL
  • GOLDENSEAL 5 [hp_X]/30mL
  • CENTELLA ASIATICA WHOLE 2 [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.
  • 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: 09-24-2020 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: 12-31-2021 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 Lympho Detox Product Label Images

Guna Lympho Detox 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

Directions

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

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

Children under 6 years: consult a physician

Active Ingredients/Purpose

AESCULUS HIPPOCASTANUM 2X HELPS VENOUS FLOWCALENDULA OFFICINALIS 1X HELPS REDUCE SWELLINGTARAXACUM OFFICINALE 1X PROMOTES URINATIONAPIS MELLIFICA 8X HELPS REDUCE SWELLINGEQUISETUM HYEMALE 3X PROMOTES URINATIONFUMARICUM ACIDUM 6X PROMOTES URINATIONGRAPHITES 12X 30X 200X DETOXIFICATIONJUGLANS REGIA 5X DETOXIFICATIONLEVOTHYROXIN 12X HELPS REDUCE SWELLINGMAGNESIA PHOSPHORICA 12X 30X 200X DETOXIFICATIONMALICUM ACIDUM 6X DETOXIFICATIONMYOSOTIS ARVENSIS 4X RELIEVES SWOLLEN LYMPH NODES, INFLAMED TONSILSNATRUM OXALACETICUM 6X DETOXIFICATIONNATRUM PYRUVICUM 6X DETOXIFICATIONPHYTOLACCA DECANDRA 4X RELIEVES SWOLLEN LYMPH NODES, INFLAMED TONSILSPLACENTA TOTALIS SUIS 6X SUPPORTS CIRCULATIONSARSAPARILLA 3X RELIEVES SWOLLEN LYMPH NODESTRICHINOYL PHOSPHATE 6X RELIEVES SWOLLEN LYMPH NODESHYDRASTIS CANADENSIS 5X RELIEVES SORE THROATHYDROCOTYLE ASIATICA 2X RELIEVES SORE THROAT

Uses

  • Helps eliminate toxins, temporarily relieves symptoms of poor lymphatic circulation, such as:swollen legsswollen lymph nodesinflamed tonsils, sore throat

Warnings

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • If pregnant or breast-feeding ask a health care professional before use.
  • Keep out of reach of children.
  • In case of overdose,seek professional assistance or contact a Poison Control Center immediately.Contains ethyl alcohol 30%

Keep out of reach of children

Pregnancy

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

Questions

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

Indications & Usage

Take 15 minutes before meals

Inactive Ingredient

Inactive ingredient: Ethyl alcohol 30%.

* Please review the disclaimer below.