NDC Package 55714-1736-1 Airway Ease

Influenzinum,Antimon. Tart.,Arsenicum Alb.,Bryonia,Chelidonium - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
55714-1736-1
Package Description:
28 g in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Airway Ease
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.
Substance Name:
Anemone Pulsatilla; Antimony Potassium Tartrate; Arctium Lappa Root; Arsenic Trioxide; Bryonia Alba Root; Chelidonium Majus; Cinchona Officinalis Bark; Drosera Anglica; Echinacea, Unspecified; Eucalyptus Gum; Goldenseal; Histamine Dihydrochloride; Influenza A Virus; Influenza B Virus; Myrrh; Phosphorus; Potassium Carbonate; Potassium Dichromate; Potassium Iodide; Rumex Crispus Root; Sambucus Nigra Flowering Top; Sodium Sulfate; Spongia Officinalis Skeleton, Roasted; Strychnos Nux-vomica Seed; Tussilago Farfara; Verbascum Thapsus
Usage Information:
Formulated for symptoms such as wheezing, shortness of breath, congestion, coughing, inflammation and other related symptoms.
11-Digit NDC Billing Format:
55714173601
Product Type:
Human Otc Drug
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.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    11-01-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55714-1736-1?

    The NDC Packaged Code 55714-1736-1 is assigned to a package of 28 g in 1 bottle, glass of Airway Ease, a human over the counter drug labeled by Newton Laboratories, Inc.. The product's dosage form is pellet and is administered via oral form.

    Is NDC 55714-1736 included in the NDC Directory?

    Yes, Airway Ease with product code 55714-1736 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on November 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55714-1736-1?

    The 11-digit format is 55714173601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-155714-1736-15-4-255714-1736-01