NDC 55714-8000 Detox

Uricum Acidum, Benzoicum Acidum, Berber. Vulg., Bryonia, Cantharis, Carduus Benedictus, Ceanothus, Chelidonium Majus, Chionanthus Virginica, Cinchona, Dioscorea, Dolichos, Iris Versicolor, Juniperus Com., Nux Vom.,ptelea,taraxacum, Carduus Mar., Cynara Scolymus, Solidago

NDC Product Code 55714-8000

NDC Code: 55714-8000

Proprietary Name: 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: Uricum Acidum, Benzoicum Acidum, Berber. Vulg., Bryonia, Cantharis, Carduus Benedictus, Ceanothus, Chelidonium Majus, Chionanthus Virginica, Cinchona, Dioscorea, Dolichos, Iris Versicolor, Juniperus Com., Nux Vom.,ptelea,taraxacum, Carduus Mar., Cynara Scolymus, Solidago 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

  • 55714 - Newton Laboratories, Inc.
    • 55714-8000 - Detox

NDC 55714-8000-1

Package Description: 29.57 mL in 1 BOTTLE, GLASS

NDC Product Information

Detox with NDC 55714-8000 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Detox is uricum acidum, benzoicum acidum, berber. vulg., bryonia, cantharis, carduus benedictus, ceanothus, chelidonium majus, chionanthus virginica, cinchona, dioscorea, dolichos, iris versicolor, juniperus com., nux vom.,ptelea,taraxacum, carduus mar., cynara scolymus, solidago. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

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.

  • URIC ACID 15 [hp_X]/mL
  • BENZOIC ACID 10 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 10 [hp_X]/mL
  • BRYONIA ALBA ROOT 10 [hp_X]/mL
  • LYTTA VESICATORIA 10 [hp_X]/mL
  • CENTAUREA BENEDICTA 10 [hp_X]/mL
  • CEANOTHUS AMERICANUS LEAF 10 [hp_X]/mL
  • CHELIDONIUM MAJUS 10 [hp_X]/mL
  • CHIONANTHUS VIRGINICUS BARK 10 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 10 [hp_X]/mL
  • DIOSCOREA VILLOSA TUBER 10 [hp_X]/mL
  • MUCUNA PRURIENS FRUIT TRICHOME 10 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 10 [hp_X]/mL
  • JUNIPER BERRY 10 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 10 [hp_X]/mL
  • PTELEA TRIFOLIATA BARK 10 [hp_X]/mL
  • TARAXACUM OFFICINALE 10 [hp_X]/mL
  • SILYBUM MARIANUM SEED 3 [hp_X]/mL
  • CYNARA SCOLYMUS LEAF 3 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL

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: Newton Laboratories, Inc.
Labeler Code: 55714
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: 04-15-2014 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: 12-31-2019 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.

Detox Product Label Images

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

Indications & Usage Section

Detox  Formulated for liver and kidney functions and for symptoms associated with toxicity such as fatigue, headaches and sluggish elimination.

Dosage & Administration Section

Directions: ORAL USE ONLY -  Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) at bedtime or as directed by a healthcare professional.  Sensitive persons begin with 1 drop and gradually increase to full dose.

Otc - Active Ingredient Section

Uricum ac. 15x, Benzoicum ac. 10x, Berber. vulg. 10x, Bryonia 10x, Cantharis 10x, Carduus ben. 10x, Ceanothus 10x, Chelidonium maj. 10x, Chionanthus 10x, Cinchona 10x, Dioscorea 10x, Dolichos 10x, Iris vers. 10x, Juniperus com. 10x, Nux vom. 10x, Ptelea 10x, Taraxacum 10x, Carduus mar. 3x, Cynara 3x, Solidago 3x, Taraxacum 3x.

Otc - Purpose Section

Formulated for liver and kidney functions and for symptoms associated with toxicity such as fatigue, headaches and sluggish elimination.

Inactive Ingredient Section

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%

Questions Section

Www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children

Otc - Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.

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