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  4. NDC Product Code: 52862-314 Total Comfort Fresh Blast

NDC 52862-314 Total Comfort Fresh Blast

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52862-314?
  4. Total Comfort Fresh Blast 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:
52862-314
Proprietary Name:
Total Comfort Fresh Blast
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
International Wholesale, Inc.
Labeler Code:
52862
Product Label ID:
cb93c5bc-9780-4cce-856a-b133580e5456
Start Marketing Date: [9]
09-28-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 52862-314?

The NDC code 52862-314 is assigned by the FDA to the product Total Comfort Fresh Blast which is product labeled by International Wholesale, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52862-314-57 57 g in 1 container . 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 Total Comfort Fresh Blast?

Apply to underams only

Which are Total Comfort Fresh Blast UNII Codes?

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

  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)

Which are Total Comfort Fresh Blast 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".