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NDC 76088-100 Invisible Solid Xtreme Anti-perspirant Deodorant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76088-100?
  4. Invisible Solid Xtreme Anti-perspirant Deodorant 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:
76088-100
Proprietary Name:
Invisible Solid Xtreme Anti-perspirant Deodorant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Import Warehouse
Labeler Code:
76088
Product Label ID:
59ac2b56-a8c0-4e44-b11d-55119ae080f1
Start Marketing Date: [9]
03-02-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76088-100-02

Package Description: 57 g in 1 CONTAINER

Product Details

What is NDC 76088-100?

The NDC code 76088-100 is assigned by the FDA to the product Invisible Solid Xtreme Anti-perspirant Deodorant which is product labeled by King Import Warehouse. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76088-100-02 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 Invisible Solid Xtreme Anti-perspirant Deodorant?

Use: Reduces underarm wetness and perspiration.

Which are Invisible Solid Xtreme Anti-perspirant Deodorant 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 Invisible Solid Xtreme Anti-perspirant Deodorant 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".