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  4. NDC Product Code: 77008-0870 Beverhill Hair Tonic

NDC 77008-0870 Beverhill Hair Tonic

Undaria Pinnatifida Extract,Camellia Sinensis Leaf Extract,Morus Alba Bark Extract,Pinus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 77008-0870?
  5. Beverhill Hair Tonic Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
77008-0870
Proprietary Name:
Beverhill Hair Tonic
Non-Proprietary Name: [1]
Undaria Pinnatifida Extract, Camellia Sinensis Leaf Extract, Morus Alba Bark Extract, Pinus Densiflora Leaf Extract, Artemisia Vulgaris Extract, Sesamum Indicum Seed Extract, Sodium Benzoate
Substance Name: [2]
Alcohol; Artemisia Vulgaris Whole; Camellia Sinensis Whole; Morus Alba Bark; Pinus Densiflora Leaf; Sesamum Indicum Whole; Sodium Benzoate; Undaria Pinnatifida
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Bioherb Co., Ltd.
    Labeler Code:
    77008
    Product Label ID:
    b07b9e2b-5cb1-7453-e053-2a95a90a996f
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    09-29-2023
    End Marketing Date: [10]
    09-28-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    BLACK (C48323)
    Shape:
    ROUND (C48348)
    Size(s):
    60 MM

    Code Structure Chart

    Product Details

    What is NDC 77008-0870?

    The NDC code 77008-0870 is assigned by the FDA to the product Beverhill Hair Tonic which is a human over the counter drug product labeled by Bioherb Co., Ltd.. The generic name of Beverhill Hair Tonic is undaria pinnatifida extract, camellia sinensis leaf extract, morus alba bark extract, pinus densiflora leaf extract, artemisia vulgaris extract, sesamum indicum seed extract, sodium benzoate. The product's dosage form is spray and is administered via topical form. The product is distributed in a single package with assigned NDC code 77008-0870-1 1 g in 1 package . 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 Beverhill Hair Tonic?

    Fluids metabolism smoothBlood metabolism smoothReducing body fatElimination of waste in bloodRemove swellingAcquiring gastrointestinal satisfactionReducing food intake

    What are Beverhill Hair Tonic 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 Beverhill Hair Tonic UNII Codes?

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

    Which are Beverhill Hair Tonic 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 Beverhill Hair Tonic?

    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".