Hay Fever Liquid
NDC Package 55714-4834-1

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 mel., echinacea, hydrastis, taraxacum, aconitum nap., alfalfa, allium cepa, ambrosia, ammon. carb., aralia rac., arsenicum alb., artemisia., arundo, bellis, berber. vulg., bryonia, calluna vulgaris, flos., chelidonium maj., chenopodium anth., cistus canadensis, drosera, dulcamara, eupatorium perf., euphrasia, fagus syl., frax. amer., gelsemium, hepar sulph. calc., histamine hydrochloricum, kali bic., kali iod., lachesis, ledum, lilium, lycopodium, nat. mur) liquids is formulated for associated symptoms of late Summer and Fall pollens such as nasal catarrh, post-nasal drip, sneezing, glandular swellings and pharyngitis. This formulation utilizes a liquid delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-4834.

Identification & Billing

NDC Package Code
55714-4834-1
Package Description
30 mL in 1 BOTTLE, GLASS
Product Code
55714-4834
11-Digit Billing Format
55714483401

Clinical Specifications

Proprietary Name
Hay Fever
Non-Proprietary Name
Apis Mel., Echinacea, Hydrastis, Taraxacum, Aconitum Nap., Alfalfa, Allium Cepa, Ambrosia, Ammon. Carb., Aralia Rac., Arsenicum Alb., Artemisia., Arundo, Bellis, Berber. Vulg., Bryonia, Calluna Vulgaris, Flos., Chelidonium Maj., Chenopodium Anth., Cistus Canadensis, Drosera, Dulcamara, Eupatorium Perf., Euphrasia, Fagus Syl., Frax. Amer., Gelsemium, Hepar Sulph. Calc., Histamine Hydrochloricum, Kali Bic., Kali Iod., Lachesis, Ledum, Lilium, Lycopodium, Nat. Mur
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; 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
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 nasal catarrh, post-nasal drip, sneezing, glandular swellings and pharyngitis.

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
09-02-2019
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 55714-4834-1 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 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; 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 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 September 02, 2019. 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: 55714483401. 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)
55714-4834-1
11-Digit CMS (5-4-2)
55714-4834-01

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