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  4. NDC Product Code: 84251-002 Wart Remover Liquid

NDC 84251-002 Wart Remover Liquid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 84251-002?
  4. Wart Remover Liquid Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing expired due to lack of listing certification.

Get all the details for National Drug Code (NDC) 84251-002 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:
84251-002
Proprietary Name:
Wart Remover Liquid
Product Type: [3]
Labeler Name: [5]
Shanghai Diguo Technology Co., Ltd
Labeler Code:
84251
Product Label ID:
1738d245-7d15-ef31-e063-6294a90a537c
FDA Application Number: [6]
M028
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
04-29-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
U
Code Navigator:

Code Structure Chart

Product Details

What is NDC 84251-002?

The NDC code 84251-002 is assigned by the FDA to the product Wart Remover Liquid which is product labeled by Shanghai Diguo Technology Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 84251-002-01 30 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 Wart Remover Liquid?

①.Please Soak the corn or warts with the warm water for 5 minutes before you use our product. ②.Clean the affected area and dry it thoroughly. Apply our product on the wart or corn with the brush or cotton swab,wait for a mask to form, then apply the liquid again. ③.Use cushions with hole centered over corn or callus to relieve pressure. ④.Repeat applying it for 2-4 weeks until the skin renews to a healthy situation.

Which are Wart Remover Liquid UNII Codes?

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

Which are Wart Remover Liquid 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

[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".