Allergies Liquid
NDC Package 55714-1519-2

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

Package Information

Allergies (apis mellifica, echinacea, hydrastis canadensis, taraxacum officinale, aconitum napellus, aethusa cynapium, agaricus muscarius, aletris farinosa, alfalfa, allium cepa, allium sativum, ambrosia artemisiaefolia, arsenicum album, artemisia vulgaris, arundo mauritanica, avena sativa, belladonna, bellis perrenis, bovista, bromium, bryonia, caffeinum, calcarea carbonica, calluna vulgaris, flos, capsicum annuum, cat hair, chamomilla, chelidonium majus, chenopodium anthelminticum, cinnamomum) liquids is formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset. This formulation utilizes a liquid delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-1519.

Identification & Billing

NDC Package Code
55714-1519-2
Package Description
50 mL in 1 BOTTLE, GLASS
Product Code
55714-1519
11-Digit Billing Format
55714151902

Clinical Specifications

Proprietary Name
Allergies
Non-Proprietary Name
Apis Mellifica, Echinacea, Hydrastis Canadensis, Taraxacum Officinale, Aconitum Napellus, Aethusa Cynapium, Agaricus Muscarius, Aletris Farinosa, Alfalfa, Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Arsenicum Album, Artemisia Vulgaris, Arundo Mauritanica, Avena Sativa, Belladonna, Bellis Perrenis, Bovista, Bromium, Bryonia, Caffeinum, Calcarea Carbonica, Calluna Vulgaris, Flos, Capsicum Annuum, Cat Hair, Chamomilla, Chelidonium Majus, Chenopodium Anthelminticum, Cinnamomum
Substance Name
Ulmus Rubra Bark; Egg Shell, Cooked; Schoenocaulon Officinale Seed; Sambucus Nigra Flowering Top; Sanguinaria Canadensis Root; Lycopus Virginicus; Lactose, Unspecified Form; Claviceps Purpurea Sclerotium; Trillium Erectum Root; Ascorbic Acid; Black Mustard Seed; Datura Stramonium; Tobacco Leaf; Allylthiourea; Urtica Urens; Elymus Repens Root; Ustilago Maydis; Wyethia Helenioides Root; Xerophyllum Asphodeloides; Apis Mellifera; Taraxacum Officinale; Aconitum Napellus; Aethusa Cynapium; Amanita Muscaria Fruiting Body; Aletris Farinosa Root; Alfalfa; Onion; Garlic; Ambrosia Artemisiifolia; Arsenic Trioxide; Artemisia Vulgaris Root; Arundo Pliniana Root; Avena Sativa Flowering Top; Atropa Belladonna; Bellis Perennis; Lycoperdon Utriforme Fruiting Body; Bromine; Bryonia Alba Root; Caffeine; Oyster Shell Calcium Carbonate, Crude; Calluna Vulgaris Flowering Top; Capsicum; Felis Catus Hair; Matricaria Chamomilla; Chelidonium Majus; Dysphania Ambrosioides; Cinnamon; Helianthemum Canadense; Protortonia Cacti; Cynara Scolymus Leaf; Canis Lupus Familiaris Hair; Drosera Anglica; Solanum Dulcamara Top; Euphrasia Stricta; Fagopyrum Esculentum; Fagus Sylvatica Nut; Alpine Strawberry; Fraxinus Americana Bark; Gelsemium Sempervirens Root; Histamine Dihydrochloride; House Dust; Hyoscyamus Niger; Abrus Precatorius Seed; Juglans Regia Leaf; Potassium Iodide; Cow Milk; Rhododendron Tomentosum Leafy Twig; Lilium Lancifolium Whole Flowering; Onosmodium Virginianum; Phytolacca Americana Root; Yucca Filamentosa; Saccharin; Echinacea, Unspecified; Goldenseal; Toxicodendron Pubescens Leaf; Salix Nigra Bark; Sulfur; Populus Balsamifera Leaf Bud; Quercus Robur Nut; Mentha Piperita; Nutmeg; Solanum Lycopersicum; Anacardium Occidentale Fruit; Ptelea Trifoliata Bark; Lycopodium Clavatum Spore; Anemone Pulsatilla; Rosa X Damascena Flowering Top; Astacus Astacus; Glycyrrhiza Glabra; Juniperus Virginiana Twig; Sucrose; Sodium Nitrate; Solanum Nigrum Whole; Solanum Tuberosum; Parthenium Hysterophorus; Ginger; Sodium Chloride; Populus Tremuloides Leaf; Corn Silk; Saccharomyces Cerevisiae
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 symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

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
01-01-2019
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (55714-1519). Click a package code to view its specific billing and regulatory data.

55714-1519-1
30 mL in 1 BOTTLE, GLASS

* 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 55714-1519-2 identifies a specific commercial package of 50 ml in 1 bottle, glass of Allergies, a human over the counter drug labeled by Newton Laboratories, Inc.. This liquid is formulated for oral use and contains ulmus rubra bark; egg shell, cooked; schoenocaulon officinale seed; sambucus nigra flowering top; sanguinaria canadensis root; lycopus virginicus; lactose, unspecified form; claviceps purpurea sclerotium; trillium erectum root; ascorbic acid; black mustard seed; datura stramonium; tobacco leaf; allylthiourea; urtica urens; elymus repens root; ustilago maydis; wyethia helenioides root; xerophyllum asphodeloides; apis mellifera; taraxacum officinale; aconitum napellus; aethusa cynapium; amanita muscaria fruiting body; aletris farinosa root; alfalfa; onion; garlic; ambrosia artemisiifolia; arsenic trioxide; artemisia vulgaris root; arundo pliniana root; avena sativa flowering top; atropa belladonna; bellis perennis; lycoperdon utriforme fruiting body; bromine; bryonia alba root; caffeine; oyster shell calcium carbonate, crude; calluna vulgaris flowering top; capsicum; felis catus hair; matricaria chamomilla; chelidonium majus; dysphania ambrosioides; cinnamon; helianthemum canadense; protortonia cacti; cynara scolymus leaf; canis lupus familiaris hair; drosera anglica; solanum dulcamara top; euphrasia stricta; fagopyrum esculentum; fagus sylvatica nut; alpine strawberry; fraxinus americana bark; gelsemium sempervirens root; histamine dihydrochloride; house dust; hyoscyamus niger; abrus precatorius seed; juglans regia leaf; potassium iodide; cow milk; rhododendron tomentosum leafy twig; lilium lancifolium whole flowering; onosmodium virginianum; phytolacca americana root; yucca filamentosa; saccharin; echinacea, unspecified; goldenseal; toxicodendron pubescens leaf; salix nigra bark; sulfur; populus balsamifera leaf bud; quercus robur nut; mentha piperita; nutmeg; solanum lycopersicum; anacardium occidentale fruit; ptelea trifoliata bark; lycopodium clavatum spore; anemone pulsatilla; rosa x damascena flowering top; astacus astacus; glycyrrhiza glabra; juniperus virginiana twig; sucrose; sodium nitrate; solanum nigrum whole; solanum tuberosum; parthenium hysterophorus; ginger; sodium chloride; populus tremuloides leaf; corn silk; saccharomyces cerevisiae 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 January 01, 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: 55714151902. 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)
55714-1519-2
11-Digit CMS (5-4-2)
55714-1519-02

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