Dizziness Liquid
NDC Package 44911-0187-1
Package Information
Dizziness (calcarea carbonica, chenopodium anthelminticum, cocculus indicus, conium maculatum, nux vomica, phosphorus, pulsatilla (pratensis), silicea, tabacum,) liquids is for temporary relief of symptoms of dizziness and light-headedness.****These statements are based upon traditional homeopathic practice. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0187.
Identification & Billing
Clinical Specifications
- ANAMIRTA COCCULUS SEED 30 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 30 [hp_X]/mL
- DYSPHANIA AMBROSIOIDES 30 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- SILICON DIOXIDE 30 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL
- TOBACCO LEAF 30 [hp_X]/mL
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0187 - Dizziness
- 44911-0187-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0187 - Dizziness
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 44911-0187-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Dizziness HP, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains anamirta cocculus seed; conium maculatum flowering top; dysphania ambrosioides; oyster shell calcium carbonate, crude; phosphorus; pulsatilla pratensis whole; silicon dioxide; strychnos nux-vomica seed; tobacco leaf 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 Energique, Inc. on July 08, 2015. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911018701. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.