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  4. NDC Product Code: 51393-7335 Wart Control Super Strength

NDC 51393-7335 Wart Control Super Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 51393-7335?
  5. Wart Control Super Strength Uses
  6. Active 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:
51393-7335
Proprietary Name:
Wart Control Super Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Forces Of Nature
Labeler Code:
51393
Product Label ID:
07edc467-28fd-40c4-a403-ef7c331d2968
Start Marketing Date: [9]
09-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Product Packages

NDC Code 51393-7335-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC Code 51393-7335-2

Package Description: 33 mL in 1 BOTTLE, DISPENSING

Product Details

What is NDC 51393-7335?

The NDC code 51393-7335 is assigned by the FDA to the product Wart Control Super Strength which is product labeled by Forces Of Nature. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51393-7335-1 11 ml in 1 bottle, dispensing , 51393-7335-2 33 ml in 1 bottle, dispensing . 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 Control Super Strength?

For the treatment of warts.

Which are Wart Control Super Strength UNII Codes?

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

* Please review the disclaimer below.

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".