Supreme Liquid
NDC 71953-0001
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Supreme (abrotanum, anacardium orientale, arsenicum album, baryta muriatica, helleborus niger, ignatia amara, lycopodium clavatum, nicotinamidum, secale cornutum, thymus (bovine), thyroidinum (bovine), calcarea carbonica, calcarea phosphorica, hypothalamus suis, pituitarum posterium (bovine), silicea) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bouari Group, Llc Dba Weight Loss Company, The. This medication is typically used as a blood coagulation factor [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 71953-0001 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
71953-0001
Proprietary Name:
Supreme
Non-Proprietary Name: [1]
Abrotanum, Anacardium Orientale, Arsenicum Album, Baryta Muriatica, Helleborus Niger, Ignatia Amara, Lycopodium Clavatum, Nicotinamidum, Secale Cornutum, Thymus (bovine), Thyroidinum (bovine), Calcarea Carbonica, Calcarea Phosphorica, Hypothalamus Suis, Pituitarum Posterium (bovine), Silicea
Substance Name: [2]
Anacardium Occidentale Fruit; Arsenic Trioxide; Artemisia Abrotanum Flowering Top; Barium Chloride Dihydrate; Bos Taurus Pituitary Gland, Posterior; Bos Taurus Thymus; Claviceps Purpurea Sclerotium; Helleborus Niger Root; Lycopodium Clavatum Spore; Niacinamide; Oyster Shell Calcium Carbonate, Crude; Silicon Dioxide; Strychnos Ignatii Seed; Sus Scrofa Hypothalamus; Thyroid, Bovine; Tribasic Calcium Phosphate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Liquid
- A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
71953
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
05-17-2018
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 71953-0001?
The NDC code 71953-0001 is assigned by the FDA to the product Supreme. It is commonly known by its generic name, abrotanum, anacardium orientale, arsenicum album, baryta muriatica, helleborus niger, ignatia amara, lycopodium clavatum, nicotinamidum, secale cornutum, thymus (bovine), thyroidinum (bovine), calcarea carbonica, calcarea phosphorica, hypothalamus suis, pituitarum posterium (bovine), silicea. This pharmaceutical product is labeled by Bouari Group, Llc Dba Weight Loss Company, The and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 71953-0001-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Helps improve diencephalic banking of fat for consumption by the body.
Helps improve diencephalic banking of fat for consumption by the body.
What are Active Ingredients of this product?
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.
- ANACARDIUM OCCIDENTALE FRUIT 6 [hp_X]/mL
- ARSENIC TRIOXIDE 6 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- ARTEMISIA ABROTANUM FLOWERING TOP 6 [hp_X]/mL
- BARIUM CHLORIDE DIHYDRATE 6 [hp_X]/mL
- BOS TAURUS PITUITARY GLAND, POSTERIOR 8 [hp_X]/mL
- BOS TAURUS THYMUS 6 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 6 [hp_X]/mL
- HELLEBORUS NIGER ROOT 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
- 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.
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
- SILICON DIOXIDE 8 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- STRYCHNOS IGNATII SEED 6 [hp_X]/mL
- SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
- THYROID, BOVINE 6 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 8 [hp_X]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
- ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E)
- ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
- HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
- THYROID, BOVINE (UNII: MN18OTN73W)
- THYROID, BOVINE (UNII: MN18OTN73W) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are the Inactive Ingredients associated 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)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".
