NDC 10096-9468 Night Magic Roll-on Anti-perspirant Deodorant

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10096-9468
Proprietary Name:
Night Magic Roll-on Anti-perspirant Deodorant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
New Avon Llc
Labeler Code:
10096
Start Marketing Date: [9]
11-12-2012
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10096-9468-1

Package Description: 50 mL in 1 BOTTLE, DISPENSING

NDC Code 10096-9468-2

Package Description: 75 mL in 1 BOTTLE, DISPENSING

Product Details

What is NDC 10096-9468?

The NDC code 10096-9468 is assigned by the FDA to the product Night Magic Roll-on Anti-perspirant Deodorant which is product labeled by New Avon Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10096-9468-1 50 ml in 1 bottle, dispensing , 10096-9468-2 75 ml in 1 bottle, dispensing . 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 Night Magic Roll-on Anti-perspirant Deodorant?

Uses•reduces underarm perspiration

Which are Night Magic Roll-on Anti-perspirant Deodorant UNII Codes?

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

  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)

* 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".