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  4. NDC Product Code: 10889-301 Dg Body Antibacterial Deodorant 3.5 Oz Bar

NDC 10889-301 Dg Body Antibacterial Deodorant 3.5 Oz Bar

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10889-301?
  5. Dg Body Antibacterial Deodorant 3.5 Oz Bar Uses
  6. Active Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10889-301
Proprietary Name:
Dg Body Antibacterial Deodorant 3.5 Oz Bar
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vvf Kansas Services Llc
Labeler Code:
10889
Product Label ID:
b3598ec2-9432-4870-bf1b-0f79c301b6ae
Start Marketing Date: [9]
07-10-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - GOLD)

Code Structure Chart

Product Details

What is NDC 10889-301?

The NDC code 10889-301 is assigned by the FDA to the product Dg Body Antibacterial Deodorant 3.5 Oz Bar 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 10889-301-02 2 soap 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 Dg Body Antibacterial Deodorant 3.5 Oz Bar?

Wet bar with waterLater vigorously and wash skinRinse and dry thoroughly

Which are Dg Body Antibacterial Deodorant 3.5 Oz Bar UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Dg Body Antibacterial Deodorant 3.5 Oz Bar?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".