NDC Package 55714-1519-1 Allergies

Apis Mellifica,Echinacea,Hydrastis Canadensis,Taraxacum Officinale,Aconitum - View Billable Units, 11-Digit Format, RxNorm

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:
55714-1519-1
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
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
Usage Information:
Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.
11-Digit NDC Billing Format:
55714151901
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):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
01-01-2019
Listing Expiration Date:
12-31-2025
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
55714-1519-250 mL in 1 BOTTLE, GLASS

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 55714-1519-1?

The NDC Packaged Code 55714-1519-1 is assigned to a package of 30 ml in 1 bottle, glass of Allergies, 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 55714-1519 included in the NDC Directory?

Yes, Allergies with product code 55714-1519 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on January 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 55714-1519-1?

The 11-digit format is 55714151901. 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
5-4-155714-1519-15-4-255714-1519-01