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  4. NDC Product Code: 49035-144 Equate Men Cool Ocean Antiperspirant

NDC 49035-144 Equate Men Cool Ocean Antiperspirant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49035-144?
  4. Equate Men Cool Ocean Antiperspirant 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:
49035-144
Proprietary Name:
Equate Men Cool Ocean Antiperspirant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wal-mart Stores, Inc.
Labeler Code:
49035
Product Label ID:
f8339911-39b2-425d-b996-65f6b1cfa0cb
Start Marketing Date: [9]
01-02-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49035-144-01

Package Description: 107 g in 1 CANISTER

Product Details

What is NDC 49035-144?

The NDC code 49035-144 is assigned by the FDA to the product Equate Men Cool Ocean Antiperspirant which is product labeled by Wal-mart Stores, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49035-144-01 107 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 Equate Men Cool Ocean Antiperspirant?

• apply to underarms only

Which are Equate Men Cool Ocean Antiperspirant UNII Codes?

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

  • ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY)
  • ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (Active Moiety)

Which are Equate Men Cool Ocean Antiperspirant 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".