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  4. NDC Product Code: 68814-489 Re-charge Black Pepper Antiperspirant Molton Brown

NDC 68814-489 Re-charge Black Pepper Antiperspirant Molton Brown

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68814-489?
  4. Re-charge Black Pepper Antiperspirant Molton Brown 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:
68814-489
Proprietary Name:
Re-charge Black Pepper Antiperspirant Molton Brown
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Molton Brown Ltd
Labeler Code:
68814
Product Label ID:
37a1a3c4-4d9b-4611-916e-d343581048a2
Start Marketing Date: [9]
11-23-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 68814-489?

The NDC code 68814-489 is assigned by the FDA to the product Re-charge Black Pepper Antiperspirant Molton Brown which is product labeled by Molton Brown Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68814-489-01 75 g in 1 cylinder . 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 Re-charge Black Pepper Antiperspirant Molton Brown?

Stop use if rash or irritation occurs

Which are Re-charge Black Pepper Antiperspirant Molton Brown UNII Codes?

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

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)

Which are Re-charge Black Pepper Antiperspirant Molton Brown 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".