64942-2397 NDC - AXE (BLACK FROZEN PEAR AND CEDARWOOD 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANT DEODORANT STICK)

Drug Information

  • Product NDC: 64942-2397
  • Proprietary Name: Axe
  • Non Proprietary Name: Black Frozen Pear and Cedarwood 48H Sweat and Odor Protection Antiperspirant Deodorant Stick
  • Active Ingredient(s): 18.2 g/100g ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
  • Administration Route(s): TOPICAL
  • Dosage Form(s): STICK

Labeler Information

Field Name Field Value
Labeler Name: Conopco, Inc. d/b/a Unilever
Product Type: HUMAN OTC DRUG
FDA Application Number: M019
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:12/1/2025

Package Information

No. Package Code Package Description Billing Unit
164942-2397-176 g in 1 CONTAINER (64942-2397-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64942-2397The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEAxeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBlack Frozen Pear and Cedarwood 48H Sweat and Odor Protection Antiperspirant Deodorant StickThis is the date that the labeler indicates was the start of its marketing of the drug product.
DOSAGE FORM NAMESTICKThis is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
ROUTE NAMETOPICALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
START MARKETING DATE12/1/2025This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGName of Company corresponding to the labeler code segment of the Product NDC.
APPLICATION NUMBERM019This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEConopco, Inc. d/b/a UnileverName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH18.2 
ACTIVE INGRED UNITg/100g 

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This page was last updated on: 3/6/2026