Allergies Pellet
NDC Package 55714-1719-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

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) pellets 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 pellet delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-1719.

Identification & Billing

NDC Package Code
55714-1719-2
Package Description
48 g in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
55714171902

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
Abrus Precatorius Seed; Aconitum Napellus; Aethusa Cynapium; Aletris Farinosa Root; Alfalfa; Allylthiourea; Alpine Strawberry; Amanita Muscaria Fruiting Body; Ambrosia Artemisiifolia; Anacardium Occidentale Fruit; Anemone Pulsatilla; Apis Mellifera; Arsenic Trioxide; Artemisia Vulgaris Root; Arundo Pliniana Root; Ascorbic Acid; Astacus Astacus; Atropa Belladonna; Avena Sativa Flowering Top; Bellis Perennis; Black Mustard Seed; Bromine; Bryonia Alba Root; Caffeine; Calluna Vulgaris Flowering Top; Canis Lupus Familiaris Hair; Capsicum; Chelidonium Majus; Cinnamon; Claviceps Purpurea Sclerotium; Corn Silk; Cow Milk; Cynara Scolymus Leaf; Datura Stramonium; Drosera Anglica; Dysphania Ambrosioides; Echinacea, Unspecified; Egg Shell, Cooked; Elymus Repens Root; Euphrasia Stricta; Fagopyrum Esculentum; Fagus Sylvatica Nut; Felis Catus Hair; Fraxinus Americana Bark; Garlic; Gelsemium Sempervirens Root; Ginger; Glycyrrhiza Glabra; Goldenseal; Helianthemum Canadense; Histamine Dihydrochloride; House Dust; Hyoscyamus Niger; Juglans Regia Leaf; Juniperus Virginiana Twig; Lactose, Unspecified Form; Lilium Lancifolium Whole Flowering; Lycoperdon Utriforme Fruiting Body; Lycopodium Clavatum Spore; Lycopus Virginicus; Matricaria Chamomilla; Mentha Piperita; Nutmeg; Onion; Onosmodium Virginianum; Oyster Shell Calcium Carbonate, Crude; Parthenium Hysterophorus; Phytolacca Americana Root; Populus Balsamifera Leaf Bud; Populus Tremuloides Leaf; Potassium Iodide; Protortonia Cacti; Ptelea Trifoliata Bark; Quercus Robur Nut; Rhododendron Tomentosum Leafy Twig; Rosa X Damascena Flowering Top; Saccharin; Saccharomyces Cerevisiae; Salix Nigra Bark; Sambucus Nigra Flowering Top; Sanguinaria Canadensis Root; Schoenocaulon Officinale Seed; Sodium Chloride; Sodium Nitrate; Solanum Dulcamara Top; Solanum Lycopersicum; Solanum Nigrum Whole; Solanum Tuberosum; Sucrose; Sulfur; Taraxacum Officinale; Tobacco Leaf; Toxicodendron Pubescens Leaf; Trillium Erectum Root; Ulmus Rubra Bark; Urtica Urens; Ustilago Maydis; Wyethia Helenioides Root; Xerophyllum Asphodeloides; Yucca Filamentosa
Dosage Form
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
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 (55714-1719). Click a package code to view its specific billing and regulatory data.

28 g 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 55714-1719-2 identifies a specific commercial package of 48 g in 1 bottle, glass of Allergies, a human over the counter drug labeled by Newton Laboratories, Inc.. This pellet is formulated for oral use and contains abrus precatorius seed; aconitum napellus; aethusa cynapium; aletris farinosa root; alfalfa; allylthiourea; alpine strawberry; amanita muscaria fruiting body; ambrosia artemisiifolia; anacardium occidentale fruit; anemone pulsatilla; apis mellifera; arsenic trioxide; artemisia vulgaris root; arundo pliniana root; ascorbic acid; astacus astacus; atropa belladonna; avena sativa flowering top; bellis perennis; black mustard seed; bromine; bryonia alba root; caffeine; calluna vulgaris flowering top; canis lupus familiaris hair; capsicum; chelidonium majus; cinnamon; claviceps purpurea sclerotium; corn silk; cow milk; cynara scolymus leaf; datura stramonium; drosera anglica; dysphania ambrosioides; echinacea, unspecified; egg shell, cooked; elymus repens root; euphrasia stricta; fagopyrum esculentum; fagus sylvatica nut; felis catus hair; fraxinus americana bark; garlic; gelsemium sempervirens root; ginger; glycyrrhiza glabra; goldenseal; helianthemum canadense; histamine dihydrochloride; house dust; hyoscyamus niger; juglans regia leaf; juniperus virginiana twig; lactose, unspecified form; lilium lancifolium whole flowering; lycoperdon utriforme fruiting body; lycopodium clavatum spore; lycopus virginicus; matricaria chamomilla; mentha piperita; nutmeg; onion; onosmodium virginianum; oyster shell calcium carbonate, crude; parthenium hysterophorus; phytolacca americana root; populus balsamifera leaf bud; populus tremuloides leaf; potassium iodide; protortonia cacti; ptelea trifoliata bark; quercus robur nut; rhododendron tomentosum leafy twig; rosa x damascena flowering top; saccharin; saccharomyces cerevisiae; salix nigra bark; sambucus nigra flowering top; sanguinaria canadensis root; schoenocaulon officinale seed; sodium chloride; sodium nitrate; solanum dulcamara top; solanum lycopersicum; solanum nigrum whole; solanum tuberosum; sucrose; sulfur; taraxacum officinale; tobacco leaf; toxicodendron pubescens leaf; trillium erectum root; ulmus rubra bark; urtica urens; ustilago maydis; wyethia helenioides root; xerophyllum asphodeloides; yucca filamentosa 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: 55714171902. 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)
55714-1719-2
11-Digit CMS (5-4-2)
55714-1719-02

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