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NDC 63479-1813 R13 Adrenal

Activated Charcoal,Causticum,Arabica Coffee Bean,Prasterone,Glycyrrhiza Glabra,Ribes - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-1813?
  4. R13 Adrenal Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
63479-1813
Proprietary Name:
R13 Adrenal
Non-Proprietary Name: [1]
Activated Charcoal, Causticum, Arabica Coffee Bean, Prasterone, Glycyrrhiza Glabra, Ribes Nigrum Flower Bud, Eleuthero, And Veratrum Album Root
Substance Name: [2]
Activated Charcoal; Arabica Coffee Bean; Causticum; Eleuthero; Glycyrrhiza Glabra; Prasterone; Ribes Nigrum Flower Bud; Veratrum Album Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s): [4]
  • Sublingual - Administration beneath the tongue.
    • Labeler Name: [5]
    Apex Energetics Inc.
    Labeler Code:
    63479
    Product Label ID:
    82bfbb2f-8487-4eda-8454-3cbb5d40bc76
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-15-1993
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 63479-1813?

    The NDC code 63479-1813 is assigned by the FDA to the product R13 Adrenal which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of R13 Adrenal is activated charcoal, causticum, arabica coffee bean, prasterone, glycyrrhiza glabra, ribes nigrum flower bud, eleuthero, and veratrum album root. The product's dosage form is solution and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-1813-1 30 ml in 1 bottle, glass . 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 R13 Adrenal?

    Adults & children ages 12 years and over: Take 10 drops under the tongue 1-3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are R13 Adrenal 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 R13 Adrenal UNII Codes?

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

    Which are R13 Adrenal 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 R13 Adrenal?

    * 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.

    [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".