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  4. NDC Product Code: 59779-983 Cvs Homeopathic Skin Tag Remover

NDC 59779-983 Cvs Homeopathic Skin Tag Remover

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59779-983?
  4. Cvs Homeopathic Skin Tag 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 data was inactivated by the FDA.
NDC Product Code:
59779-983
Proprietary Name:
Cvs Homeopathic Skin Tag Remover
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy, Inc
Labeler Code:
59779
Product Label ID:
adc2b575-8093-4e2c-ab32-8beb15d3674c
Start Marketing Date: [9]
06-25-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 59779-983?

The NDC code 59779-983 is assigned by the FDA to the product Cvs Homeopathic Skin Tag Remover which is product labeled by Cvs Pharmacy, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-983-00 1 bottle, glass in 1 package / 10 ml in 1 bottle, glass. 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 Cvs Homeopathic Skin Tag Remover?

Apply 3 times daily to affected area.  Skin tags will dry and flake away over several week period.  Some individuals may be sensitive to essential oil.  Skin test for tolerability.  If irritation or reaction occurs, discontinue use.

Which are Cvs Homeopathic Skin Tag Remover UNII Codes?

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

  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)

Which are Cvs Homeopathic Skin Tag 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".