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  4. NDC Product Code: 83299-006 Wart Remover

NDC 83299-006 Wart Remover

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83299-006?
  4. Wart Remover 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 certification is expired.
NDC Product Code:
83299-006
Proprietary Name:
Wart Remover
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Consilii Llc
Labeler Code:
83299
Product Label ID:
fd363916-d1f9-9681-e053-6294a90a0b1e
Start Marketing Date: [9]
06-02-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 83299-006?

The NDC code 83299-006 is assigned by the FDA to the product Wart Remover which is product labeled by Consilii Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83299-006-01 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 Wart Remover?

Wash the affected area may soak the wart in warm water for 5 minutes dry area thoroughly using the applicator(brush or cotton swab), apply one drop at a time to sufficiently cover each wart allow it to fully absorb and let dry repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks

Which are Wart Remover UNII Codes?

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

Which are Wart Remover 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.

[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 ("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".