NDC 83027-0001 Dizzy Formula
Arnica Montana,Hydrocotyle Asiatica,Ambra Grisea,Argentum Nitricum,Cocculus Indicus,Conium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83027 - Nutritional Specialties, Inc.
- 83027-0001 - Dizzy Formula
Product Packages
NDC Code 83027-0001-1
Package Description: 60 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 83027-0001?
What are the uses for Dizzy Formula?
What are Dizzy Formula Active Ingredients?
- AMBERGRIS 12 [hp_X]/mL - A gray substance found in the GASTROINTESTINAL TRACT of the SPERM WHALE.
- ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
- ARNICA MONTANA WHOLE 3 [hp_X]/mL
- CANIS LUPUS FAMILIARIS MILK 12 [hp_X]/mL
- CENTELLA ASIATICA FLOWERING TOP 3 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- SILVER NITRATE 12 [hp_X]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
- THERIDION CURASSAVICUM 18 [hp_X]/mL
Which are Dizzy Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- CENTELLA ASIATICA FLOWERING TOP (UNII: J02K2IV2PB)
- CENTELLA ASIATICA FLOWERING TOP (UNII: J02K2IV2PB) (Active Moiety)
- AMBERGRIS (UNII: XTC0D02P6C)
- AMBERGRIS (UNII: XTC0D02P6C) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (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)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (Active Moiety)
- THERIDION CURASSAVICUM (UNII: 9Z8D3HEM8L)
- THERIDION CURASSAVICUM (UNII: 9Z8D3HEM8L) (Active Moiety)
Which are Dizzy Formula 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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 ("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".