NDC 55714-4796 Dust-mold-dander

Iris Versicolor, Solidago Virgaurea, Antimonium Crudum, Apis Mellifica, Arsenicum Album, Baptisia Tinctoria, Blatta Orientalis, Bromium, Bryonia, Candida Albicans, Carduus Benedictus, Cat Hair, Chelidonium Majus, Cinchona Officinalis, Dog Hair, Histaminum Hydrochloricum, House Dust, Ipecacuanha, Lycopodium Clavatum, Nux Vomica, Podophyllum Peltatum, Rhus Toxicodendron, Secale Cornutum, Silicea, Ustilago Maidis, Torula Cerevisiae.

NDC Product Code 55714-4796

NDC CODE: 55714-4796

Proprietary Name: Dust-mold-dander 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: Iris Versicolor, Solidago Virgaurea, Antimonium Crudum, Apis Mellifica, Arsenicum Album, Baptisia Tinctoria, Blatta Orientalis, Bromium, Bryonia, Candida Albicans, Carduus Benedictus, Cat Hair, Chelidonium Majus, Cinchona Officinalis, Dog Hair, Histaminum Hydrochloricum, House Dust, Ipecacuanha, Lycopodium Clavatum, Nux Vomica, Podophyllum Peltatum, Rhus Toxicodendron, Secale Cornutum, Silicea, Ustilago Maidis, Torula Cerevisiae. 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.

  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).

NDC Code Structure

  • 55714 - Newton Laboratories, Inc.

NDC 55714-4796-1

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC Product Information

Dust-mold-dander with NDC 55714-4796 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Dust-mold-dander is iris versicolor, solidago virgaurea, antimonium crudum, apis mellifica, arsenicum album, baptisia tinctoria, blatta orientalis, bromium, bryonia, candida albicans, carduus benedictus, cat hair, chelidonium majus, cinchona officinalis, dog hair, histaminum hydrochloricum, house dust, ipecacuanha, lycopodium clavatum, nux vomica, podophyllum peltatum, rhus toxicodendron, secale cornutum, silicea, ustilago maidis, torula cerevisiae.. 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.

Dust-mold-dander 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.

  • HOUSE DUST 20 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 11 [hp_X]/mL
  • ANTIMONY TRISULFIDE 20 [hp_X]/mL
  • APIS MELLIFERA 20 [hp_X]/mL
  • ARSENIC TRIOXIDE 20 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 20 [hp_X]/mL
  • BLATTA ORIENTALIS 20 [hp_X]/mL
  • BROMINE 20 [hp_X]/mL
  • BRYONIA ALBA ROOT 20 [hp_X]/mL
  • CANDIDA ALBICANS 20 [hp_X]/mL
  • CENTAUREA BENEDICTA 20 [hp_X]/mL
  • FELIS CATUS HAIR 20 [hp_X]/mL
  • CHELIDONIUM MAJUS 20 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 20 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS HAIR 20 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 20 [hp_X]/mL
  • IPECAC 20 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 20 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 20 [hp_X]/mL
  • PODOPHYLLUM 20 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 20 [hp_X]/mL
  • CLAVICEPS PURPUREA SCLEROTIUM 20 [hp_X]/mL
  • SILICON DIOXIDE 20 [hp_X]/mL
  • USTILAGO MAYDIS 20 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE 21 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 11 [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.

  • WATER (UNII: 059QF0KO0R)
  • 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: 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: 09-02-2019 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.

Dust-mold-dander Product Label Images

Dust-mold-dander 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

Formulated for associated symptoms such as nasal congestions, post-nasal drip, sneezing and sore throat.

Otc - Purpose Section

Formulated for associated symptoms such as nasal congestion, post-nasal drip, sneezing and sore throat.

Inactive Ingredient Section

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

Questions Section

Newtonlabs.net - Questions? 800.448.7256Newton Laboratories, Inc. FDA Est # 1051203 Conyers, GA 30013

Warnings Section

WARNINGS: 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.

Otc - Pregnancy Or Breast Feeding Section

If
pregnant or breast-feeding, ask a doctor before use.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.