Motion Sickness Hp Liquid
NDC Package 43406-0099-1

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

Package Information

Motion Sickness Hp (arnica montana, bryonia alba root, quinine sulfate, anamirta cocculus seed, conium maculatum flowering top, strychnos ignatii seed, ipecac, potassium carbonate, strychnos nux-vomica seed, sepia officinalis juice, tobacco leaf, veratrum album root) liquids is uSES: Temporarily relieves symptoms related to motion sickness. This formulation utilizes a liquid delivery system. Marketed by Natural Creations, Inc., this product is identified by NDC 43406-0099.

Identification & Billing

NDC Package Code
43406-0099-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
11-Digit Billing Format
43406009901

Clinical Specifications

Proprietary Name
Motion Sickness Hp
Non-Proprietary Name
Arnica Montana, Bryonia Alba Root, Quinine Sulfate, Anamirta Cocculus Seed, Conium Maculatum Flowering Top, Strychnos Ignatii Seed, Ipecac, Potassium Carbonate, Strychnos Nux-vomica Seed, Sepia Officinalis Juice, Tobacco Leaf, Veratrum Album Root
Substance Name
Anamirta Cocculus Seed; Arnica Montana; Bryonia Alba Root; Conium Maculatum Flowering Top; Ipecac; Potassium Carbonate; Quinine Sulfate; Sepia Officinalis Juice; Strychnos Ignatii Seed; Strychnos Nux-vomica Seed; Tobacco Leaf; Veratrum Album Root
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.
Usage Information
USES: Temporarily relieves symptoms related to motion sickness.

Regulatory & Marketing

Labeler Name
Natural Creations, 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
05-29-2007
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 43406-0099-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Motion Sickness Hp, a human over the counter drug labeled by Natural Creations, Inc.. This liquid is formulated for oral use and contains anamirta cocculus seed; arnica montana; bryonia alba root; conium maculatum flowering top; ipecac; potassium carbonate; quinine sulfate; sepia officinalis juice; strychnos ignatii seed; strychnos nux-vomica seed; tobacco leaf; veratrum album root 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 Natural Creations, Inc. on May 29, 2007. The current certification is valid through December 31, 2026.

How is this Natural Creations, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43406009901. 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)
43406-0099-1
11-Digit CMS (5-4-2)
43406-0099-01

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