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  4. NDC Product Code: 51815-217 Soft And Dri Dri Gel Soft Scent

NDC 51815-217 Soft And Dri Dri Gel Soft Scent

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51815-217?
  4. Soft And Dri Dri Gel Soft Scent 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:
51815-217
Proprietary Name:
Soft And Dri Dri Gel Soft Scent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vvf Illinois Services
Labeler Code:
51815
Product Label ID:
9272aced-e17b-4359-89ca-d1e2a2a8ae72
Start Marketing Date: [9]
01-01-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51815-217-00

Package Description: 85 g in 1 PACKAGE

Product Details

What is NDC 51815-217?

The NDC code 51815-217 is assigned by the FDA to the product Soft And Dri Dri Gel Soft Scent which is product labeled by Vvf Illinois Services. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51815-217-00 85 g in 1 package . 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 Soft And Dri Dri Gel Soft Scent?

Apply to underarms only

Which are Soft And Dri Dri Gel Soft Scent 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 Soft And Dri Dri Gel Soft Scent 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".