NDC 77008-0870 Beverhill Hair Tonic

Undaria Pinnatifida Extract, Camellia Sinensis Leaf Extract, Morus Alba Bark Extract, Pinus Densiflora Leaf Extract, Artemisia Vulgaris Extract, Sesamum Indicum Seed Extract, Sodium Benzoate

NDC Product Code 77008-0870

NDC CODE: 77008-0870

Proprietary Name: Beverhill Hair Tonic What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Undaria Pinnatifida Extract, Camellia Sinensis Leaf Extract, Morus Alba Bark Extract, Pinus Densiflora Leaf Extract, Artemisia Vulgaris Extract, Sesamum Indicum Seed Extract, Sodium Benzoate 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.

Product Characteristics

BLACK (C48323)
Shape: ROUND (C48348)
60 MM

NDC Code Structure

  • 77008 - Bioherb Co., Ltd.

NDC 77008-0870-1

Package Description: 1 g in 1 PACKAGE

NDC Product Information

Beverhill Hair Tonic with NDC 77008-0870 is a 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.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Beverhill Hair Tonic Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bioherb Co., Ltd.
Labeler Code: 77008
Marketing Category: UNAPPROVED DRUG OTHER - 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.

Start Marketing Date: 09-28-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 09-29-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Beverhill Hair Tonic Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

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

Otc - Keep Out Of Reach Of Children


These Highlights Do Not Include All The Information Needed To Use. See Full Prescribing Information.

Serving Size: 1 bottle (60mL)Serving size 1 bottle, 3-4 times a day


Warning: For adult-use only

Otc - Purpose

Improves hair-loss

Inactive Ingredient

Inactive ingredients:Laminaria Cloustoni ExtractGlycine Soja (Soybean) Seed Extract

Poria Cocos Extract
Rehmannia Chinensis Root Extract

Thuja Orientalis Leaf Extract




Otc - Active Ingredient

Active IngredientsWater

Undaria Pinnatifida ExtractCamellia Sinensis Leaf Extract Morus Alba Bark Extract

Pinus Densiflora Leaf Extract

Artemisia Vulgaris Extract
Sesamum Indicum (Sesame) Seed Extract

Sodium Benzoate

Recent Major Changes

1 package: 1 bottle(60mL)

Address: 140, Donyu-2ro, Moonsan-eup, Paju-si, Gyeonggi-do, S.Korea

* Please review the disclaimer below.