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  4. NDC Product Code: 44911-0187 Dizziness HP

NDC 44911-0187 Dizziness HP

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0187?
  4. Dizziness HP Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 44911-0187 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
44911-0187
Proprietary Name:
Dizziness HP
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
0bf53ecc-c2ad-40b5-b921-7c10a1b00626
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
07-08-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 44911-0187?

The NDC code 44911-0187 is assigned by the FDA to the product Dizziness HP which is product labeled by Energique, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44911-0187-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Dizziness HP?

For temporary relief of symptoms of dizziness and light-headedness.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms of dizziness and light-headedness.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Which are Dizziness HP UNII Codes?

The UNII codes for the active ingredients in this product are:

  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • DYSPHANIA AMBROSIOIDES (UNII: 4H5RSU087I)
  • CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (Active Moiety)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • PULSATILLA PRATENSIS (UNII: 8E272251DI)
  • PULSATILLA PRATENSIS (UNII: 8E272251DI) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • TOBACCO LEAF (UNII: 6YR2608RSU)
  • TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)

Which are Dizziness HP Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".