NDC 63505-160 Fraicheur Bambou Antiperspirant And Deodorant Roll-on

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:
63505-160
Proprietary Name:
Fraicheur Bambou Antiperspirant And Deodorant Roll-on
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yves Rocher North America Inc
Labeler Code:
63505
Start Marketing Date: [9]
10-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63505-160-08

Package Description: 60 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 63505-160?

The NDC code 63505-160 is assigned by the FDA to the product Fraicheur Bambou Antiperspirant And Deodorant Roll-on which is product labeled by Yves Rocher North America Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63505-160-08 60 ml in 1 bottle, plastic . 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 Fraicheur Bambou Antiperspirant And Deodorant Roll-on?

UseReduces underarm perspiration

Which are Fraicheur Bambou Antiperspirant And Deodorant Roll-on UNII Codes?

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

  • ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V)
  • ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (Active Moiety)

Which are Fraicheur Bambou Antiperspirant And Deodorant Roll-on 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:

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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".