NDC 81488-007 Mineffect Hangover Relief
Alumina Silicata,Calcarea Silicata,Silicea,Ferrum Metallicum,Ferrum Phosphoricum,Ferrum - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 81488-007?
What are the uses for Mineffect Hangover Relief?
What are Mineffect Hangover Relief Active Ingredients?
- CALCIUM SILICATE 5 [hp_X]/59mL
- FERRIC CHLORIDE HEXAHYDRATE 7 [hp_X]/59mL
- FERROSOFERRIC PHOSPHATE 7 [hp_X]/59mL
- IRON 7 [hp_X]/59mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
- KAOLIN 5 [hp_X]/59mL - The most common mineral of a group of hydrated aluminum silicates, approximately H2Al2Si2O8-H2O. It is prepared for pharmaceutical and medicinal purposes by levigating with water to remove sand, etc. (From Merck Index, 11th ed) The name is derived from Kao-ling (Chinese: "high ridge"), the original site. (From Grant & Hackh's Chemical Dictionary, 5th ed)
- PHOSPHORUS 6 [hp_X]/59mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- SILICON DIOXIDE 4 [hp_X]/59mL - 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.
- SULFUR 4 [hp_X]/59mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
Which are Mineffect Hangover Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- KAOLIN (UNII: 24H4NWX5CO)
- KAOLIN (UNII: 24H4NWX5CO) (Active Moiety)
- CALCIUM SILICATE (UNII: S4255P4G5M)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- FERRIC CHLORIDE HEXAHYDRATE (UNII: 0I2XIN602U)
- FERRIC CATION (UNII: 91O4LML611) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
Which are Mineffect Hangover Relief 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)
- CEROUS OXALATE NONAHYDRATE (UNII: 0UV74P3R0J)
- POTASSIUM SILICATE (UNII: J86L1GUL6K)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)
- SODIUM NITRATE (UNII: 8M4L3H2ZVZ)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ZINC (UNII: J41CSQ7QDS)
Which are the Pharmacologic Classes for Mineffect Hangover Relief?
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Iron - [CS]
- Parenteral Iron Replacement - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
* 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".