1. Home
  2. Labeler Index
  3. Jiangxi Hemei Pharmaceutical Co., Ltd
  4. NDC Product Code: 84010-135 Bldaxn Fungal Nail Renewal

NDC 84010-135 Bldaxn Fungal Nail Renewal

Undecylenic Acid 25% Fungal Nail Renewal Liquid Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 84010-135?
  4. Bldaxn Fungal Nail Renewal 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) 84010-135 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:
84010-135
Proprietary Name:
Bldaxn Fungal Nail Renewal
Non-Proprietary Name: [1]
Undecylenic Acid 25% Fungal Nail Renewal
Substance Name: [2]
Undecylenic Acid
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]
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]
Jiangxi Hemei Pharmaceutical Co., Ltd
Labeler Code:
84010
Product Label ID:
37e8c837-4e5d-d380-e063-6294a90a6aad
FDA Application Number: [6]
M005
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
06-19-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 84010-135?

The NDC code 84010-135 is assigned by the FDA to the product Bldaxn Fungal Nail Renewal which is a human over the counter drug product labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. The generic name of Bldaxn Fungal Nail Renewal is undecylenic acid 25% fungal nail renewal. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 84010-135-01 2 bottle in 1 box / 15 ml 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 Bldaxn Fungal Nail Renewal?

·Wash feet thoroughly with warm water, and gently file the thickened part of the nail with a nail file until it is flat. ·Apply a layer of the liquid to the surface of the nail and allow it to be absorbed.Repeat the process twice a day. ·Use it continuously for at least 4 weeks to see an effect. ·For complete improvement, we recommend using it for 6 weeks or more. (Only for adults and children 12 years and over)

What are Bldaxn Fungal Nail Renewal 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 Bldaxn Fungal Nail Renewal UNII Codes?

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

Which are Bldaxn Fungal Nail Renewal 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:

* 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.

[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".