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NDC 87130-001 Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin

Reishi,Schisandra Chinensis Seed,Maritime Pine Powder Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 87130-001?
  4. Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin 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) 87130-001 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:
87130-001
Proprietary Name:
Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin
Non-Proprietary Name: [1]
Reishi, Schisandra Chinensis Seed, Maritime Pine
Substance Name: [2]
Maritime Pine; Reishi; Schisandra Chinensis Seed
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Japan Medical Biotechnology Limited
Labeler Code:
87130
Product Label ID:
41941041-0af3-3d37-e063-6294a90accb5
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]
10-20-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 87130-001?

The NDC code 87130-001 is assigned by the FDA to the product Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin which is a human over the counter drug product labeled by Japan Medical Biotechnology Limited. The generic name of Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin is reishi, schisandra chinensis seed, maritime pine. The product's dosage form is powder and is administered via oral form. The product is distributed in 2 packages with assigned NDC codes 87130-001-01 10 bottle in 1 box / 6 g in 1 bottle, 87130-001-02 90 bottle in 1 box / 6 g 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 Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin?

Ages 18-39: 6g every 12 hours; not more than 12g in 24hoursAges 40-65: 6g every 8 hours; not more than 18g in 24hours

What are Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin 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.
  • MARITIME PINE 120 mg/6g - A plant genus in the family PINACEAE, order Pinales, class Pinopsida, division Coniferophyta. They are evergreen trees mainly in temperate climates.
  • REISHI 2271 mg/6g - A mushroom, Ganoderma lucidum, of the POLYPORALES order of basidiomycetous fungi. It has long been used in traditional Chinese medicine in various forms.
  • SCHISANDRA CHINENSIS SEED 120 mg/6g

Which are Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin UNII Codes?

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

Which are Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin 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.

[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".