1. Labeler Index
  2. Ventura Corporation, Ltd.
  3. NDC Product Code: 13537-156 Esika Total Sec Ultra Fresh

NDC 13537-156 Esika Total Sec Ultra Fresh

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 13537-156?
    4. Esika Total Sec Ultra Fresh 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:
13537-156
Proprietary Name:
Esika Total Sec Ultra Fresh
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ventura Corporation, Ltd.
Labeler Code:
13537
Product Label ID:
011b9494-b2c4-490d-94e9-e9624d3b5c83
Start Marketing Date: [9]
01-24-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 13537-156-01

Package Description: 50 mL in 1 BOTTLE

Product Details

What is NDC 13537-156?

The NDC code 13537-156 is assigned by the FDA to the product Esika Total Sec Ultra Fresh which is product labeled by Ventura Corporation, Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 13537-156-01 50 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 Esika Total Sec Ultra Fresh?

Apply to underarms only.

Which are Esika Total Sec Ultra Fresh UNII Codes?

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

  • ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V)
  • ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (Active Moiety)

Which are Esika Total Sec Ultra Fresh 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

[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".