Hay Fever Liquid
NDC Package 55714-2562-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Hay Fever (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) liquids is formulated for associated symptoms of late Summer and Fall pollens such as itchy eyes, sneezing, post-nasal drip, sore throat and sinus pressure. This formulation utilizes a liquid delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-2562.

Identification & Billing

NDC Package Code
55714-2562-1
Package Description
30 mL in 1 BOTTLE, GLASS
Product Code
55714-2562
11-Digit Billing Format
55714256201

Clinical Specifications

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
Lilium Lancifolium Whole Flowering; Sodium Chloride; Populus Balsamifera Leaf Bud; Anemone Pulsatilla; Eupatorium Perfoliatum Flowering Top; Euphrasia Stricta; Gelsemium Sempervirens Root; Onosmodium Virginianum; Schoenocaulon Officinale Seed; Sanguinaria Canadensis Root; Solidago Virgaurea Flowering Top; Trillium Erectum Root; Ulmus Rubra Bark; Histamine Dihydrochloride; Xerophyllum Asphodeloides; Ustilago Maydis; Parthenium Hysterophorus; Potassium Iodide; Lycopodium Clavatum Spore; Populus Tremuloides Leaf; Rosa X Damascena Flowering Top; Salix Nigra Bark; Elymus Repens Root; Datura Stramonium; Urtica Urens; Wyethia Helenioides Root; Quercus Robur Nut; Apis Mellifera; Goldenseal; Taraxacum Officinale; Aconitum Napellus; Alfalfa; Onion; Ambrosia Artemisiifolia; Ammonium Carbonate; Aralia Racemosa Root; Arsenic Trioxide; Artemisia Vulgaris Root; Arundo Pliniana Root; Bellis Perennis; Berberis Vulgaris Root Bark; Bryonia Alba Root; Calluna Vulgaris Flowering Top; Chelidonium Majus; Dysphania Ambrosioides; Helianthemum Canadense; Drosera Anglica; Solanum Dulcamara Top; Echinacea, Unspecified; Fagus Sylvatica Nut; Fraxinus Americana Bark; Calcium Sulfide; Potassium Dichromate; Lachesis Muta Venom; Rhododendron Tomentosum Leafy Twig
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
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.

Regulatory & Marketing

Labeler Name
Newton Laboratories, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
05-18-2020
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55714-2562-1 identifies a specific commercial package of 30 ml in 1 bottle, glass of Hay Fever, a human over the counter drug labeled by Newton Laboratories, Inc.. This liquid is formulated for oral use and contains lilium lancifolium whole flowering; sodium chloride; populus balsamifera leaf bud; anemone pulsatilla; eupatorium perfoliatum flowering top; euphrasia stricta; gelsemium sempervirens root; onosmodium virginianum; schoenocaulon officinale seed; sanguinaria canadensis root; solidago virgaurea flowering top; trillium erectum root; ulmus rubra bark; histamine dihydrochloride; xerophyllum asphodeloides; ustilago maydis; parthenium hysterophorus; potassium iodide; lycopodium clavatum spore; populus tremuloides leaf; rosa x damascena flowering top; salix nigra bark; elymus repens root; datura stramonium; urtica urens; wyethia helenioides root; quercus robur nut; apis mellifera; goldenseal; taraxacum officinale; aconitum napellus; alfalfa; onion; ambrosia artemisiifolia; ammonium carbonate; aralia racemosa root; arsenic trioxide; artemisia vulgaris root; arundo pliniana root; bellis perennis; berberis vulgaris root bark; bryonia alba root; calluna vulgaris flowering top; chelidonium majus; dysphania ambrosioides; helianthemum canadense; drosera anglica; solanum dulcamara top; echinacea, unspecified; fagus sylvatica nut; fraxinus americana bark; calcium sulfide; potassium dichromate; lachesis muta venom; rhododendron tomentosum leafy twig as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Newton Laboratories, Inc. on May 18, 2020. The current certification is valid through December 31, 2026.

How is this Newton Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55714256201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
55714-2562-1
11-Digit CMS (5-4-2)
55714-2562-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.