NDC 55714-4639 Multi-system

Aspergillus Niger, Cladosporium, Candida Albicans, Thyroidinum, Ustilago Maidis, Aconitum Nap., Antimonium Tart. Aralia Quinquefolia, Arnica, Arsenicum Alb., Baptisia, Bryonia, Cantharis, Chelidonium Majus, Cinchona, Echinacea, Iodium, Kali Carb. Kali Iod., Lachesis, Lycopodium Lycopus Virginicus, Nat. Mur., Nux Vom., Phosphorus, Phytolacca, Pulsatilla, Rhus Toxicodendron, Sabal

NDC Product Code 55714-4639

NDC Code: 55714-4639

Proprietary Name: Multi-system 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: Aspergillus Niger, Cladosporium, Candida Albicans, Thyroidinum, Ustilago Maidis, Aconitum Nap., Antimonium Tart. Aralia Quinquefolia, Arnica, Arsenicum Alb., Baptisia, Bryonia, Cantharis, Chelidonium Majus, Cinchona, Echinacea, Iodium, Kali Carb. Kali Iod., Lachesis, Lycopodium Lycopus Virginicus, Nat. Mur., Nux Vom., Phosphorus, Phytolacca, Pulsatilla, Rhus Toxicodendron, Sabal 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.
    • 55714-4639 - Multi-system

NDC 55714-4639-1

Package Description: 28 g in 1 BOTTLE, GLASS

NDC Product Information

Multi-system with NDC 55714-4639 is a a human prescription drug product labeled by Newton Laboratories, Inc.. The generic name of Multi-system is aspergillus niger, cladosporium, candida albicans, thyroidinum, ustilago maidis, aconitum nap., antimonium tart. aralia quinquefolia, arnica, arsenicum alb., baptisia, bryonia, cantharis, chelidonium majus, cinchona, echinacea, iodium, kali carb. kali iod., lachesis, lycopodium lycopus virginicus, nat. mur., nux vom., phosphorus, phytolacca, pulsatilla, rhus toxicodendron, sabal. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.

Product Type: Human Prescription 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.

Multi-system 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.

  • ASPERGILLUS NIGER VAR. NIGER 15 [hp_X]/g
  • CLADOSPORIUM HERBARUM 15 [hp_X]/g
  • CANDIDA ALBICANS 15 [hp_X]/g
  • THYROID, UNSPECIFIED 15 [hp_X]/g
  • USTILAGO MAYDIS 15 [hp_X]/g
  • ACONITUM NAPELLUS 10 [hp_X]/g
  • ANTIMONY POTASSIUM TARTRATE 10 [hp_X]/g
  • AMERICAN GINSENG 10 [hp_X]/g
  • ARNICA MONTANA 10 [hp_X]/g
  • ARSENIC TRIOXIDE 10 [hp_X]/g
  • BAPTISIA TINCTORIA 10 [hp_X]/g
  • BRYONIA ALBA ROOT 10 [hp_X]/g
  • LYTTA VESICATORIA 10 [hp_X]/g
  • CHELIDONIUM MAJUS 10 [hp_X]/g
  • CINCHONA OFFICINALIS BARK 10 [hp_X]/g
  • ECHINACEA, UNSPECIFIED 10 [hp_X]/g
  • IODINE 10 [hp_X]/g
  • POTASSIUM CARBONATE 10 [hp_X]/g
  • POTASSIUM IODIDE 10 [hp_X]/g
  • LACHESIS MUTA VENOM 10 [hp_X]/g
  • LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/g
  • LYCOPUS VIRGINICUS 10 [hp_X]/g
  • SODIUM CHLORIDE 10 [hp_X]/g
  • STRYCHNOS NUX-VOMICA SEED 10 [hp_X]/g
  • PHOSPHORUS 10 [hp_X]/g
  • PHYTOLACCA AMERICANA ROOT 10 [hp_X]/g
  • PULSATILLA VULGARIS 10 [hp_X]/g
  • TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/g
  • SAW PALMETTO 10 [hp_X]/g

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.

  • SUCROSE (UNII: C151H8M554)

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.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Fungal Proteins - [CS]
  • Allergens - [CS]
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Fungal Proteins - [CS]
  • Allergens - [CS]
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Fungal Proteins - [CS]
  • Allergens - [CS]
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Fungal Proteins - [CS]
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]

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: 04-17-2017 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.

Multi-system Product Label Images

Multi-system 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

Keep Out Of Reach Of Children Section

Keep out of reach of children.

Warnings Section

Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If
pregnant or breast-feeding,​ ask a doctor before use.

Questions Section

Www.newtonlabs.net Newton laboratories, Inc. FDA Est# 1051203 - Conyers, GA 30013. Questions? 1.800.448.7256

Inactive Ingredient Section

Gluten-free, non-GMO, organic beet-derived sucrose (lactose-free) pellets.

Purpose Section

Formulated for symptoms such as Valley Fever, Gulf War Syndrome, environmental sensitivity and other related conditions.

Active Ingredient Section

Equal parts of Aconitum nap. 10x, Antimonium tart. 10x, Aralia quinquefolia 10x, Arnica 10x, Arsenicum alb. 10x, Baptisia 10x, Bryonia 10x, Cantharis 10x, Chelidonium majus 10x, Cinchona 10x, Echinacea 10x, Iodum 10x, Kali carb. 10x, Kali iod. 10x, Lachesis 10x, Lycopodium 10x, Lycopus virginicus 10x, Nat. mur. 10x, Nux vom. 10x, Phosphorous 10x, Phytolacca 10x, Pulsatilla 10x, Rhus toxicodendron 10x, Sabal 10x, Allersodes 15x, Candida albicans 15x, Thyroidinum 15x, Ustilago maidis 15x.

Dosage & Administration Section

Directions: Ages 12 and up, take 6 pellets by mouth (ages 0 - 11, give 3 pellets) four times daily or as directed by a health professional. Under age 2, crush or dissolve pellets in purified water.

Indications & Usage Section

Formulated for symptoms associated with Valley Fever, Gulf War Syndrome, environmental sensitivity and other related conditions.

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.

* Please review the disclaimer below.

Previous Code
55714-4638
Next Code
55714-4640