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  5. NDC Package Code: 55714-4776-1 Broncare

NDC Package 55714-4776-1 Broncare

Echinacea,Lappa,Rumex Crisp.,Antimon. Tart.,Arsenicum Alb.,Bryonia,Camphora,Chelidonium - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
55714-4776-1
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
55714-4776
Proprietary Name:
Broncare
Non-Proprietary Name:
Echinacea, Lappa, Rumex Crisp., Antimon. Tart., Arsenicum Alb., Bryonia, Camphora, Chelidonium Maj., Cinchona, Drosera, Eucalyptus, Hepar Sulph. Calc., Histaminum Hydrochloricum, Ipecac., Kali Bic., Kali Carb., Kali Iod., Lycopodium, Myrrha, Nat. Sulphuricum, Nux Vom., Phos., Pulsatilla, Sainguinaria, Spongia, Stannum Met., Tussilago Far., Verbascum, Influenzinum
Substance Name:
Anemone Pulsatilla; Antimony Potassium Tartrate; Arctium Lappa Root; Arsenic Trioxide; Bryonia Alba Root; Calcium Sulfide; Camphor (natural); Chelidonium Majus; Cinchona Officinalis Bark; Drosera Anglica; Echinacea, Unspecified; Eucalyptus Gum; Histamine Dihydrochloride; Influenza A Virus; Influenza B Virus; Ipecac; Lycopodium Clavatum Spore; Myrrh; Phosphorus; Potassium Carbonate; Potassium Dichromate; Potassium Iodide; Rumex Crispus Root; Sanguinaria Canadensis Root; Sodium Sulfate; Spongia Officinalis Skeleton, Roasted; Strychnos Nux-vomica Seed; Tin; Tussilago Farfara; Verbascum Thapsus
Usage Information:
Formulated for symptoms such as excess mucus, cough, congestion, and shortness of breath.
11-Digit NDC Billing Format:
55714477601
Product Type:
Human Otc Drug
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.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ANEMONE PULSATILLA 15 [hp_X]/mL
  • ANTIMONY POTASSIUM TARTRATE 15 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • CALCIUM SULFIDE 15 [hp_X]/mL
  • CAMPHOR (NATURAL) 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 15 [hp_X]/mL
  • DROSERA ANGLICA 15 [hp_X]/mL
  • ECHINACEA, UNSPECIFIED 6 [hp_X]/mL
  • EUCALYPTUS GUM 15 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 15 [hp_X]/mL
  • INFLUENZA A VIRUS 30 [hp_X]/mL
  • INFLUENZA B VIRUS 30 [hp_X]/mL
  • IPECAC 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • MYRRH 15 [hp_X]/mL
  • PHOSPHORUS 15 [hp_X]/mL
  • POTASSIUM CARBONATE 15 [hp_X]/mL
  • POTASSIUM DICHROMATE 15 [hp_X]/mL
  • POTASSIUM IODIDE 15 [hp_X]/mL
  • RUMEX CRISPUS ROOT 6 [hp_X]/mL
  • SANGUINARIA CANADENSIS ROOT 15 [hp_X]/mL
  • SODIUM SULFATE 15 [hp_X]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • TIN 15 [hp_X]/mL
  • TUSSILAGO FARFARA 15 [hp_X]/mL
  • VERBASCUM THAPSUS 15 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-02-2019
    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 55714-4776-1?

    The NDC Packaged Code 55714-4776-1 is assigned to a package of 30 ml in 1 bottle, glass of Broncare, a human over the counter drug labeled by Newton Laboratories, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 55714-4776 included in the NDC Directory?

    Yes, Broncare with product code 55714-4776 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on September 02, 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 55714-4776-1?

    The 11-digit format is 55714477601. 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
    5-4-155714-4776-15-4-255714-4776-01