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  4. NDC Product Code: 62795-1042 Reboost

NDC 62795-1042 Reboost

Aconitum Napellus,Bryonia Alba Root,Eupatorium Perfoliatum Flowering - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62795-1042?
  5. Reboost Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
62795-1042
Proprietary Name:
Reboost
Non-Proprietary Name: [1]
Aconitum Napellus, Bryonia Alba Root, Eupatorium Perfoliatum Flowering Top, Goldenseal, Lachesis Muta Venom, Phosphorus, Vincetoxicum Hirundinaria Root, Zinc Gluconate, Zinc Acetate Anhydrous, Cairina Moschata Heart/liver Autolysate, Ipecac, Sulfur And Influenza A Virus A/singapore/6/86 (h1n1) Antigen (heat Inactivated)
Substance Name: [2]
Aconitum Napellus; Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Eupatorium Perfoliatum Flowering Top; Goldenseal; Influenza A Virus A/singapore/6/86 (h1n1) Antigen (heat Inactivated); Ipecac; Lachesis Muta Venom; Phosphorus; Sulfur; Vincetoxicum Hirundinaria Root; Zinc Acetate Anhydrous; Zinc Gluconate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Medinatura Inc.
    Labeler Code:
    62795
    Product Label ID:
    37da8f7b-5a42-4f1b-b227-612d152e21f5
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-19-2020
    End Marketing Date: [10]
    04-30-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    9 MM
    Imprint(s):
    SUN
    Score:
    1
    Flavor(s):
    LEMON (C73396)

    Product Packages

    NDC Code 62795-1042-2

    Package Description: 1 BOTTLE in 1 CARTON / 60 TABLET in 1 BOTTLE

    Product Details

    What is NDC 62795-1042?

    The NDC code 62795-1042 is assigned by the FDA to the product Reboost which is a human over the counter drug product labeled by Medinatura Inc.. The generic name of Reboost is aconitum napellus, bryonia alba root, eupatorium perfoliatum flowering top, goldenseal, lachesis muta venom, phosphorus, vincetoxicum hirundinaria root, zinc gluconate, zinc acetate anhydrous, cairina moschata heart/liver autolysate, ipecac, sulfur and influenza a virus a/singapore/6/86 (h1n1) antigen (heat inactivated). The product's dosage form is tablet and is administered via oral form. The product is distributed in a single package with assigned NDC code 62795-1042-2 1 bottle in 1 carton / 60 tablet in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Reboost?

    Directions: For max absorption, dissolve undertongue. Can be chewed and swallowed. Adults andchildren 12 years and older: 2 tablets every 4 hours.Do not exceed 12 tablets per 24 hours. Children 4 to11 years: 1-2 tablets every 4 hours. Do not exceed12 tablets per 24 hours. For children under 4 years,consult your health professional.

    What are Reboost Active Ingredients?

    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.

    Which are Reboost UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
    • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
    • GOLDENSEAL (UNII: ZW3Z11D0JV)
    • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
    • PHOSPHORUS (UNII: 27YLU75U4W)
    • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
    • VINCETOXICUM HIRUNDINARIA ROOT (UNII: 9R858U917W)
    • CYNANCHUM VINCETOXICUM ROOT (UNII: 9R858U917W) (Active Moiety)
    • ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
    • ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
    • ZINC ACETATE ANHYDROUS (UNII: H2ZEY72PME)
    • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
    • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
    • IPECAC (UNII: 62I3C8233L)
    • IPECAC (UNII: 62I3C8233L) (Active Moiety)
    • SULFUR (UNII: 70FD1KFU70)
    • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
    • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) ANTIGEN (HEAT INACTIVATED) (UNII: WC4E824FQ9)
    • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: DRA5YV248Q) (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:

    Which are the Pharmacologic Classes for Reboost?

    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.

    * Please review the disclaimer below.

    Product Footnotes

    [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.

    [10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

    [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".