1. Home
  2. Labeler Index
  3. Aramis Inc.
  4. NDC Product Code: 42472-001 24 Hour Antiperspirant Natural

NDC 42472-001 24 Hour Antiperspirant Natural

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42472-001?
  4. 24 Hour Antiperspirant Natural 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:
42472-001
Proprietary Name:
24 Hour Antiperspirant Natural
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aramis Inc.
Labeler Code:
42472
Product Label ID:
e4fb57cc-94fc-420c-916b-3e9681cf5707
Start Marketing Date: [9]
10-01-1979
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 42472-001?

The NDC code 42472-001 is assigned by the FDA to the product 24 Hour Antiperspirant Natural which is product labeled by Aramis Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42472-001-01 81 ml in 1 bottle, spray . 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 24 Hour Antiperspirant Natural?

USE: REDUCES UNDERARM WETNESS

Which are 24 Hour Antiperspirant Natural UNII Codes?

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

  • ALUMINUM CHLOROHYDREX PROPYLENE GLYCOL (UNII: PGG6VG42HP)
  • ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)

Which are 24 Hour Antiperspirant Natural 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".