1. Home
  2. Labeler Index
  3. Newton Laboratories, Inc.
  4. 55714-2562
  5. NDC Package Code: 55714-2562-1 Hay Fever

NDC Package 55714-2562-1 Hay Fever

Apis Mellifica,Echinacea,Hydrastis Canadensis,Taraxacum Officinale,Aconitum - 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:
55714-2562-1
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
55714-2562
Proprietary Name:
Hay Fever
Non-Proprietary Name:
Apis Mellifica, Echinacea, Hydrastis Canadensis, Taraxacum Officinale, Aconitum Napellus, Alfalfa, Allium Cepa, Ambrosia Artemisiaefolia, Ammonium Carbonicum, Aralia Racemosa, Arsenicum Album, Artemisia Vulgaris, Arundo Mauritanica, Bellis Perennis, Berberis Vulgaris, Bryonia, Calluna Vulgaris, Flos, Chelidonium Majus, Chenopodium Anthelminticum, Cistus Canadensis, Drosera, Dulcamara, Eupatorium Perfoliatum, Euphrasia Officinalis, Fagus Sylvatica, Fraxinus Americana, Gelsemium Sempervirens
Substance Name:
Aconitum Napellus; Alfalfa; Ambrosia Artemisiifolia; Ammonium Carbonate; Anemone Pulsatilla; Apis Mellifera; Aralia Racemosa Root; Arsenic Trioxide; Artemisia Vulgaris Root; Arundo Pliniana Root; Bellis Perennis; Berberis Vulgaris Root Bark; Bryonia Alba Root; Calcium Sulfide; Calluna Vulgaris Flowering Top; Chelidonium Majus; Datura Stramonium; Drosera Anglica; Dysphania Ambrosioides; Echinacea, Unspecified; Elymus Repens Root; Eupatorium Perfoliatum Flowering Top; Euphrasia Stricta; Fagus Sylvatica Nut; Fraxinus Americana Bark; Gelsemium Sempervirens Root; Goldenseal; Helianthemum Canadense; Histamine Dihydrochloride; Lachesis Muta Venom; Lilium Lancifolium Whole Flowering; Lycopodium Clavatum Spore; Onion; Onosmodium Virginianum; Parthenium Hysterophorus; Populus Balsamifera Leaf Bud; Populus Tremuloides Leaf; Potassium Dichromate; Potassium Iodide; Quercus Robur Nut; Rhododendron Tomentosum Leafy Twig; Rosa X Damascena Flowering Top; Salix Nigra Bark; Sanguinaria Canadensis Root; Schoenocaulon Officinale Seed; Sodium Chloride; Solanum Dulcamara Top; Solidago Virgaurea Flowering Top; Taraxacum Officinale; Trillium Erectum Root; Ulmus Rubra Bark; Urtica Urens; Ustilago Maydis; Wyethia Helenioides Root; Xerophyllum Asphodeloides
Usage Information:
Formulated for associated symptoms of late Summer and Fall pollens such as itchy eyes, sneezing, post-nasal drip, sore throat and sinus pressure.
11-Digit NDC Billing Format:
55714256201
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):
  • ACONITUM NAPELLUS 15 [hp_X]/mL
  • ALFALFA 15 [hp_X]/mL
  • AMBROSIA ARTEMISIIFOLIA 15 [hp_X]/mL
  • AMMONIUM CARBONATE 15 [hp_X]/mL
  • ANEMONE PULSATILLA 15 [hp_X]/mL
  • APIS MELLIFERA 6 [hp_X]/mL
  • ARALIA RACEMOSA ROOT 15 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • ARTEMISIA VULGARIS ROOT 15 [hp_X]/mL
  • ARUNDO PLINIANA ROOT 15 [hp_X]/mL
  • BELLIS PERENNIS 15 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • CALCIUM SULFIDE 15 [hp_X]/mL
  • CALLUNA VULGARIS FLOWERING TOP 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • DATURA STRAMONIUM 15 [hp_X]/mL
  • DROSERA ANGLICA 15 [hp_X]/mL
  • DYSPHANIA AMBROSIOIDES 15 [hp_X]/mL
  • ECHINACEA, UNSPECIFIED 6 [hp_X]/mL
  • ELYMUS REPENS ROOT 15 [hp_X]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 15 [hp_X]/mL
  • EUPHRASIA STRICTA 15 [hp_X]/mL
  • FAGUS SYLVATICA NUT 15 [hp_X]/mL
  • FRAXINUS AMERICANA BARK 15 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 15 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • HELIANTHEMUM CANADENSE 15 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 15 [hp_X]/mL
  • LACHESIS MUTA VENOM 15 [hp_X]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • ONION 15 [hp_X]/mL
  • ONOSMODIUM VIRGINIANUM 15 [hp_X]/mL
  • PARTHENIUM HYSTEROPHORUS 16 [hp_X]/mL
  • POPULUS BALSAMIFERA LEAF BUD 15 [hp_X]/mL
  • POPULUS TREMULOIDES LEAF 15 [hp_X]/mL
  • POTASSIUM DICHROMATE 15 [hp_X]/mL
  • POTASSIUM IODIDE 15 [hp_X]/mL
  • QUERCUS ROBUR NUT 15 [hp_X]/mL
  • RHODODENDRON TOMENTOSUM LEAFY TWIG 15 [hp_X]/mL
  • ROSA X DAMASCENA FLOWERING TOP 15 [hp_X]/mL
  • SALIX NIGRA BARK 15 [hp_X]/mL
  • SANGUINARIA CANADENSIS ROOT 15 [hp_X]/mL
  • SCHOENOCAULON OFFICINALE SEED 15 [hp_X]/mL
  • SODIUM CHLORIDE 15 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 15 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 15 [hp_X]/mL
  • TARAXACUM OFFICINALE 6 [hp_X]/mL
  • TRILLIUM ERECTUM ROOT 15 [hp_X]/mL
  • ULMUS RUBRA BARK 16 [hp_X]/mL
  • URTICA URENS 15 [hp_X]/mL
  • USTILAGO MAYDIS 15 [hp_X]/mL
  • WYETHIA HELENIOIDES ROOT 15 [hp_X]/mL
  • XEROPHYLLUM ASPHODELOIDES 15 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Bee Venoms - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Fungal Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Vegetable Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-18-2020
    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 55714-2562-1?

    The NDC Packaged Code 55714-2562-1 is assigned to a package of 30 ml in 1 bottle, glass of Hay Fever, 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 55714-2562 included in the NDC Directory?

    Yes, Hay Fever with product code 55714-2562 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on May 18, 2020 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 55714-2562-1?

    The 11-digit format is 55714256201. 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
    5-4-155714-2562-15-4-255714-2562-01