NDC 62795-4004 Reboost
Apis Mellifera,Atropa Belladonna,Zinc Gluconate,Baptisia Tinctoria Root,Ulmus Rubra - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62795 - Medinatura
- 62795-4004 - Reboost
Product Packages
NDC Code 62795-4004-9
Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 20 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 62795-4004?
What are the uses for Reboost?
What are Reboost Active Ingredients?
- APIS MELLIFERA 6 [hp_X]/20mL
- ATROPA BELLADONNA 5 [hp_X]/20mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BAPTISIA TINCTORIA ROOT 1 [hp_X]/20mL
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 20 [hp_X]/20mL
- CALENDULA OFFICINALIS FLOWERING TOP 4 [hp_X]/20mL
- ECHINACEA PURPUREA 4 [hp_X]/20mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- GOLDENSEAL 5 [hp_X]/20mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/20mL
- PLANTAGO MAJOR 3 [hp_X]/20mL
- SAGE 3 [hp_X]/20mL
- SULFUR 4 [hp_X]/20mL - 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.
- ULMUS RUBRA BARK 1 [hp_X]/20mL
- VINCETOXICUM HIRUNDINARIA ROOT 6 [hp_X]/20mL
- ZINC ACETATE ANHYDROUS 4 [hp_X]/20mL - A salt produced by the reaction of zinc oxide with acetic acid and used as an astringent, styptic, and emetic.
- ZINC GLUCONATE 1 [hp_X]/20mL
Which are Reboost UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- SAGE (UNII: 065C5D077J)
- SAGE (UNII: 065C5D077J) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- ULMUS RUBRA BARK (UNII: 91QY4PXU8Q)
- ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- ZINC ACETATE ANHYDROUS (UNII: H2ZEY72PME)
- VINCETOXICUM HIRUNDINARIA ROOT (UNII: 9R858U917W)
- CYNANCHUM VINCETOXICUM ROOT (UNII: 9R858U917W) (Active Moiety)
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
Which are Reboost 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:
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- FRUCTOSE (UNII: 6YSS42VSEV)
- WATER (UNII: 059QF0KO0R)
- CHERRY (UNII: BUC5I9595W)
Which are the Pharmacologic Classes for Reboost?
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
* 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".