NDC 55714-1736 Airway Ease

Influenzinum, Antimon. Tart., Arsenicum Alb., Bryonia, Chelidonium Majus, Cinchona, Drosera, Eucalyptus, Histaminum Hydrochloricum, Hydrastis, Kali Bic., Kali Carb., Kali Iod., Myrrha, Nat. Sulphuricum, Nux Vom., Phosphorus, Pulsatilla, Rumex Crisp., Sambucus Nig., Spongia, Tussilago Farfara, Verbascum, Echinacea, Lappa.

NDC Product Code 55714-1736

NDC CODE: 55714-1736

Proprietary Name: Airway Ease 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: Influenzinum, Antimon. Tart., Arsenicum Alb., Bryonia, Chelidonium Majus, Cinchona, Drosera, Eucalyptus, Histaminum Hydrochloricum, Hydrastis, Kali Bic., Kali Carb., Kali Iod., Myrrha, Nat. Sulphuricum, Nux Vom., Phosphorus, Pulsatilla, Rumex Crisp., Sambucus Nig., Spongia, Tussilago Farfara, Verbascum, Echinacea, Lappa. 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.

NDC 55714-1736-1

Package Description: 28 g in 1 BOTTLE, GLASS

NDC Product Information

Airway Ease with NDC 55714-1736 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Airway Ease is influenzinum, antimon. tart., arsenicum alb., bryonia, chelidonium majus, cinchona, drosera, eucalyptus, histaminum hydrochloricum, hydrastis, kali bic., kali carb., kali iod., myrrha, nat. sulphuricum, nux vom., phosphorus, pulsatilla, rumex crisp., sambucus nig., spongia, tussilago farfara, verbascum, echinacea, lappa.. 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 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.

Airway Ease 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.

  • SAMBUCUS NIGRA FLOWERING TOP 15 [hp_X]/g
  • INFLUENZA A VIRUS 30 [hp_X]/g
  • ANTIMONY POTASSIUM TARTRATE 15 [hp_X]/g
  • ARSENIC TRIOXIDE 15 [hp_X]/g
  • BRYONIA ALBA ROOT 15 [hp_X]/g
  • CHELIDONIUM MAJUS 15 [hp_X]/g
  • CINCHONA OFFICINALIS BARK 15 [hp_X]/g
  • DROSERA ANGLICA 15 [hp_X]/g
  • EUCALYPTUS GUM 15 [hp_X]/g
  • HISTAMINE DIHYDROCHLORIDE 15 [hp_X]/g
  • GOLDENSEAL 15 [hp_X]/g
  • POTASSIUM DICHROMATE 15 [hp_X]/g
  • POTASSIUM CARBONATE 15 [hp_X]/g
  • POTASSIUM IODIDE 15 [hp_X]/g
  • MYRRH 15 [hp_X]/g
  • SODIUM SULFATE 15 [hp_X]/g
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/g
  • PHOSPHORUS 15 [hp_X]/g
  • ANEMONE PULSATILLA 15 [hp_X]/g
  • RUMEX CRISPUS ROOT 15 [hp_X]/g
  • SPONGIA OFFICINALIS SKELETON, ROASTED 15 [hp_X]/g
  • TUSSILAGO FARFARA 15 [hp_X]/g
  • VERBASCUM THAPSUS 15 [hp_X]/g
  • ECHINACEA, UNSPECIFIED 6 [hp_X]/g
  • ARCTIUM LAPPA ROOT 6 [hp_X]/g
  • INFLUENZA B VIRUS 30 [hp_X]/g

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: 11-01-2019 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: 12-31-2020 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.

Airway Ease Product Label Images