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  5. NDC Package Code: 55714-4780-1 Dizzi-v

NDC Package 55714-4780-1 Dizzi-v

Absinthium,Aconitum Nap.,Antimon. Tart.,Belladonna,Bryonia,Carbolicum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
55714-4780-1
Package Description:
28 g in 1 BOTTLE, GLASS
Product Code:
55714-4780
Proprietary Name:
Dizzi-v
Non-Proprietary Name:
Absinthium, Aconitum Nap., Antimon. Tart., Belladonna, Bryonia, Carbolicum Acidum, Colchicum, Conium, Ferrum Metallicum, Gelsemium, Glonoinum, Hyoscyamus, Ipecac., Iris Versicolor, Lycopodium, Nux Vom., Petroleum, Phosphorus, Sepia, Symphoricarpus Racemosus, Tabacum, Theridion, Zingiber, Echinacea, Hypericum, Passiflora, Valeriana
Substance Name:
Aconitum Napellus; Antimony Potassium Tartrate; Atropa Belladonna; Bryonia Alba Root; Colchicum Autumnale Bulb; Conium Maculatum Flowering Top; Echinacea, Unspecified; Gelsemium Sempervirens Root; Ginger; Hyoscyamus Niger; Hypericum Perforatum; Ipecac; Iris Versicolor Root; Iron; Kerosene; Lycopodium Clavatum Spore; Nitroglycerin; Passiflora Incarnata Flowering Top; Phenol; Phosphorus; Sepia Officinalis Juice; Strychnos Nux-vomica Seed; Symphoricarpos Albus Fruit; Theridion Curassavicum; Tobacco Leaf; Valerian; Wormwood
Usage Information:
Formulated for symptoms such as dizziness, nausea and sensations of motion, spinning or floating.
11-Digit NDC Billing Format:
55714478001
Product Type:
Human Otc Drug
Labeler Name:
Newton Laboratories, Inc.
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(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:
09-02-2019
Listing Expiration Date:
12-31-2026
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 55714-4780-1?

The NDC Packaged Code 55714-4780-1 is assigned to a package of 28 g in 1 bottle, glass of Dizzi-v, a human over the counter drug labeled by Newton Laboratories, Inc.. The product's dosage form is pellet and is administered via oral form.

Is NDC 55714-4780 included in the NDC Directory?

Yes, Dizzi-v with product code 55714-4780 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on September 02, 2019 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 55714-4780-1?

The 11-digit format is 55714478001. 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
5-4-155714-4780-15-4-255714-4780-01