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  4. NDC Product Code: 10889-103 Dead Down Wind Scentprevent Antiperspirant

NDC 10889-103 Dead Down Wind Scentprevent Antiperspirant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10889-103?
  4. Dead Down Wind Scentprevent Antiperspirant Uses
  5. Active 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:
10889-103
Proprietary Name:
Dead Down Wind Scentprevent Antiperspirant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vvf Kansas Services Llc
Labeler Code:
10889
Product Label ID:
92380b63-78da-44ef-b05d-2015a04bd3b0
Start Marketing Date: [9]
08-15-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 10889-103?

The NDC code 10889-103 is assigned by the FDA to the product Dead Down Wind Scentprevent Antiperspirant which is product labeled by Vvf Kansas Services Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10889-103-12 1 stick 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 Dead Down Wind Scentprevent Antiperspirant?

This product is used as Anti-Perspirant. Reduces underarm wetness.To Use Turn dial to raise product. Apply to underarms. Replace cap.

Which are Dead Down Wind Scentprevent Antiperspirant UNII Codes?

The UNII codes for the active 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".