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  4. NDC Product Code: 64776-696 Scent Killer Anti-perspirant And Deodorant Odorless Formula

NDC 64776-696 Scent Killer Anti-perspirant And Deodorant Odorless Formula

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64776-696?
  4. Scent Killer Anti-perspirant And Deodorant Odorless Formula 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:
64776-696
Proprietary Name:
Scent Killer Anti-perspirant And Deodorant Odorless Formula
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wildlife Research Center, Inc.
Labeler Code:
64776
Product Label ID:
b0859381-495e-4943-95f8-854df5c5b680
Start Marketing Date: [9]
04-08-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 64776-696?

The NDC code 64776-696 is assigned by the FDA to the product Scent Killer Anti-perspirant And Deodorant Odorless Formula which is product labeled by Wildlife Research Center, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64776-696-01 64 g in 1 canister . 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 Scent Killer Anti-perspirant And Deodorant Odorless Formula?

Use:Reduces underarm wetness and perspiration.

Which are Scent Killer Anti-perspirant And Deodorant Odorless Formula UNII Codes?

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

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)

Which are Scent Killer Anti-perspirant And Deodorant Odorless Formula 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".