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  4. NDC Product Code: 41595-5441 Sure Conditioning Solid Vitamin Infusion

NDC 41595-5441 Sure Conditioning Solid Vitamin Infusion

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41595-5441?
  4. Sure Conditioning Solid Vitamin Infusion 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:
41595-5441
Proprietary Name:
Sure Conditioning Solid Vitamin Infusion
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Idelle Labs, Ltd
Labeler Code:
41595
Product Label ID:
dbb991d5-951d-4fcd-b5b2-950dda27e257
Start Marketing Date: [9]
08-23-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41595-5441-2

Package Description: 73 g in 1 CANISTER

NDC Code 41595-5441-4

Package Description: 93 g in 1 CANISTER

Product Details

What is NDC 41595-5441?

The NDC code 41595-5441 is assigned by the FDA to the product Sure Conditioning Solid Vitamin Infusion which is product labeled by Idelle Labs, Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 41595-5441-2 73 g in 1 canister , 41595-5441-4 93 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 Sure Conditioning Solid Vitamin Infusion?

Apply to underarms only

Which are Sure Conditioning Solid Vitamin Infusion UNII Codes?

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

  • ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH)
  • ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (Active Moiety)

Which are Sure Conditioning Solid Vitamin Infusion 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".