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  4. NDC Product Code: 44911-0181 Vertitone

NDC 44911-0181 Vertitone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0181?
  4. Vertitone 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.
NDC Product Code:
44911-0181
Proprietary Name:
Vertitone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
12f1c465-b64a-446c-a28c-e96dabe03580
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 44911-0181?

The NDC code 44911-0181 is assigned by the FDA to the product Vertitone 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 44911-0181-1 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 Vertitone?

For temporary relief of dizziness, motion sickness with nausea.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For temporary relief of dizziness, motion sickness with nausea.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Which are Vertitone UNII Codes?

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

  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
  • AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (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)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • PULSATILLA PRATENSIS (UNII: 8E272251DI)
  • PULSATILLA PRATENSIS (UNII: 8E272251DI) (Active Moiety)

Which are Vertitone 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:

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Product Footnotes

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

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".