NDC 64942-1224 Dove Cleartone Pink Antiperspirant 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:
64942-1224
Proprietary Name:
Dove Cleartone Pink Antiperspirant Deodorant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Conopco Inc. D/b/a Unilever
Labeler Code:
64942
Start Marketing Date: [9]
01-26-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 64942-1224-1

Package Description: 74 g in 1 CONTAINER

NDC Code 64942-1224-2

Package Description: 45 g in 1 CONTAINER

NDC Code 64942-1224-3

Package Description: 14 g in 1 CONTAINER

Product Details

What is NDC 64942-1224?

The NDC code 64942-1224 is assigned by the FDA to the product Dove Cleartone Pink Antiperspirant Deodorant which is product labeled by Conopco Inc. D/b/a Unilever. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 64942-1224-1 74 g in 1 container , 64942-1224-2 45 g in 1 container , 64942-1224-3 14 g in 1 container . 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 Dove Cleartone Pink Antiperspirant Deodorant?

Uses/Para usos  · reduces underarm wetness/ reduce la sudoración de la axila· 24 hour protection/24 horas/Hrs de protección

Which are Dove Cleartone Pink Antiperspirant Deodorant UNII Codes?

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

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)

Which are Dove Cleartone Pink Antiperspirant Deodorant 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".