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  4. NDC Product Code: 87325-001 Bestwe Hair Growth Tonic

NDC 87325-001 Bestwe Hair Growth Tonic

Duckweed Extract, Panax Ginseng Root, Platycladus Orientalis Seeds Extract, Ginger - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 87325-001?
  4. Bestwe Hair Growth Tonic Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 87325-001 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
87325-001
Proprietary Name:
Bestwe Hair Growth Tonic
Non-Proprietary Name: [1]
Duckweed Extract, Panax Ginseng Root, Platycladus Orientalis Seeds Extract, Ginger Extract, Radix Polygoni Multiflori Extract, Cnidium Fruit Seeds Extract, Glossy Privet Fruit Extract
Substance Name: [2]
Cnidium Monnieri Fruit; Lemna Minor; Ligustrum Lucidum Fruit; Panax Ginseng Root; Platycladus Orientalis Seed; Polygonum Cuspidatum Root; Zingiber Officinale (ginger) Root Oil
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Percutaneous - Administration through the skin.
Labeler Name: [5]
Yantai Dupont Daily Necessities Co., Ltd.
Labeler Code:
87325
Product Label ID:
47c49ccd-b648-a749-e063-6394a90a1dd9
FDA Application Number: [6]
505G(a)(3)
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
01-07-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 87325-001?

The NDC code 87325-001 is assigned by the FDA to the product Bestwe Hair Growth Tonic which is a human over the counter drug product labeled by Yantai Dupont Daily Necessities Co., Ltd.. The generic name of Bestwe Hair Growth Tonic is duckweed extract, panax ginseng root, platycladus orientalis seeds extract, ginger extract, radix polygoni multiflori extract, cnidium fruit seeds extract, glossy privet fruit extract. The product's dosage form is liquid and is administered via percutaneous form. The product is distributed in a single package with assigned NDC code 87325-001-01 99 g in 1 bottle, plastic . 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 Bestwe Hair Growth Tonic?

Spray on the target area and do massage for more than 10 seconds. ■ Use for hair regrowth ■ Use for Anti-Hair Loss

What are Bestwe Hair Growth 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 Bestwe Hair Growth Tonic UNII Codes?

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

  • ZINGIBER OFFICINALE (GINGER) ROOT OIL (UNII: SAS9Z1SVUK)
  • ZINGIBER OFFICINALE (GINGER) ROOT OIL (UNII: SAS9Z1SVUK) (Active Moiety)
  • POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
  • POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7) (Active Moiety)
  • PANAX GINSENG ROOT (UNII: CUQ3A77YXI)
  • PANAX GINSENG ROOT (UNII: CUQ3A77YXI) (Active Moiety)
  • LIGUSTRUM LUCIDUM FRUIT (UNII: M9G2U96DUT)
  • LIGUSTRUM LUCIDUM FRUIT (UNII: M9G2U96DUT) (Active Moiety)
  • CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
  • CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS) (Active Moiety)
  • LEMNA MINOR (UNII: 621HHM46SV)
  • LEMNA MINOR (UNII: 621HHM46SV) (Active Moiety)
  • PLATYCLADUS ORIENTALIS SEED (UNII: QDB7SF78HO)
  • PLATYCLADUS ORIENTALIS SEED (UNII: QDB7SF78HO) (Active Moiety)

Which are Bestwe Hair Growth 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:

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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".