NDC 80814-0002 Ultra Slim 30
Fucus Vesiculosus,Cysteinum,Nicotinamidum,Alpha-lipoicum Acidum,Antimonium Crudum,Chromium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80814 - H2 Nutrition
- 80814-0002 - Ultra Slim 30
Product Packages
NDC Code 80814-0002-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 80814-0002?
What are the uses for Ultra Slim 30?
What are Ultra Slim 30 Active Ingredients?
- ALPHA LIPOIC ACID 12 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
- ANTIMONY TRISULFIDE 12 [hp_X]/mL
- CHROMIC SULFATE PENTADECAHYDRATE 12 [hp_X]/mL
- CYSTEINE 6 [hp_X]/mL - A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
- FUCUS VESICULOSUS 3 [hp_X]/mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
- GAMBOGE 12 [hp_X]/mL - A plant genus of the family CLUSIACEAE. Members contain XANTHONES.
- GRAPHITE 30 [hp_C]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- NIACINAMIDE 6 [hp_X]/mL - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
- SEMECARPUS ANACARDIUM JUICE 30 [hp_C]/mL
Which are Ultra Slim 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- CYSTEINE (UNII: K848JZ4886)
- CYSTEINE (UNII: K848JZ4886) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- CHROMIC SULFATE PENTADECAHYDRATE (UNII: E4T8TU3LE8)
- CHROMIC CATION (UNII: X1N4508KF1) (Active Moiety)
- GAMBOGE (UNII: 7556HJ7587)
- GAMBOGE (UNII: 7556HJ7587) (Active Moiety)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
Which are Ultra Slim 30 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:
- AMERICAN GINSENG (UNII: 8W75VCV53Q)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GARCINIA GUMMI-GUTTA FRUIT (UNII: D0QJI8UQVR)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R)
- LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
- PLECTRANTHUS BARBATUS ROOT (UNII: V5741391RG)
- GUGGUL (UNII: 34969JX79R)
- 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".